Skip to main content

BRIEF RESEARCH REPORT article

Front. Psychiatry, 14 September 2023
Sec. Sleep Disorders
This article is part of the Research Topic New Insights into Sleep Abnormalities Associated with Alcohol, Cannabis, Cocaine, and Opiate use View all 5 articles

Patient reported preferences for sleep interventions among women receiving buprenorphine for opioid use disorder

\r\nMichelle Eglovitch
Michelle Eglovitch1*Anna Beth Parlier-AhmadAnna Beth Parlier-Ahmad1Catherine LeggeCatherine Legge2Sajanee ChithranjanSajanee Chithranjan2Saisriya KolliSaisriya Kolli2Stephanie ViolanteStephanie Violante1Joseph M. DzierzewskiJoseph M. Dzierzewski3Andrew Stephen HuhnAndrew Stephen Huhn4Allison WilkersonAllison Wilkerson5Caitlin Eileen Martin,Caitlin Eileen Martin6,7
  • 1Department of Psychology, Virginia Commonwealth University, Richmond, VA, United States
  • 2School of Medicine, Virginia Commonwealth University, Richmond, VA, United States
  • 3National Sleep Foundation, Washington, DC, United States
  • 4School of Medicine, Johns Hopkins University, Baltimore, MD, United States
  • 5Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, United States
  • 6Institute for Drug and Alcohol Studies, Virginia Commonwealth University, Richmond, VA, United States
  • 7Department of Obstetrics and Gynecology, School of Medicine, Virginia Commonwealth University, Richmond, VA, United States

Aim: Among individuals receiving medication for OUD (MOUD), insomnia is highly prevalent and increases the risk for negative OUD outcomes. However, little is known about MOUD patient-reported preferences for insomnia treatments among women with OUD. This mixed-methods study explored acceptability of and patient preferences for sleep interventions among women in OUD treatment.

Methods: This is an analysis from an ongoing cross-sectional survey and interview study investigating the relationship between sleep and OUD recovery. The parent study is actively enrolling non-pregnant women between 18–45 years stabilized on buprenorphine from an outpatient program. Participants complete measures including the Insomnia Severity Index (ISI), with scores of ≥10 identifying clinically significant insomnia symptoms. A sub-sample who met this threshold completed semi-structured interviews. Descriptive statistics were generated for survey responses, and applied thematic analysis was used for interview data.

Results: Participants selected for the qualitative interview (n = 11) highlighted prior positive and negative experiences with sleep treatments, challenges with employing non-pharmacological sleep strategies, and preferences for both medical and behavioral sleep interventions while in recovery. Women emphasized the need for flexibility of sleep therapy sessions to align with ongoing social determinants (e.g., caregiving responsibilities) as well as for sleep medications without sedating effects nor risk of dependency.

Conclusions: Many women receiving MOUD have concomitant insomnia symptoms, and desire availability of both pharmacologic and behavioral sleep interventions within the OUD treatment setting. Qualitative findings underscore the need for evidence-based sleep interventions that account for the unique socioenvironmental factors that may impact strategy implementation in this population.

Introduction

The overdose crisis continues to be a serious public health concern, largely due to opioid-related deaths, which increased 345% between 2001 and 2016 (1, 2). Opioid use disorder (OUD) remains a leading cause of morbidity and mortality. Medication for opioid use disorder (MOUD) is a life-saving treatment shown to reduce overdose risk and improve health outcomes (3). However, heterogeneity in MOUD outcomes persist and discontinuation rates remain high, at least in part due to social determinants of health and comorbid health conditions, underscoring the urgent need for evidence to guide improvements in the quality of OUD treatments.

Among individuals receiving MOUD, sleep disturbances, such as insomnia, are highly prevalent and likely increase risk for substance use recurrence and other negative recovery outcomes, such as reduced quality of life (4, 5). Current prevalence estimates of sleep disorders in people on MOUD range from 19 to 41% (6). Emerging evidence suggests multiple underlying mechanisms of this bi-directional relationship between sleep and OUD treatment trajectories, including increased impulsivity, heightened stress response, chronic pain, and persistent cravings. Additionally, sleep disturbance may interfere with learning during behavioral therapies, compromising patients' abilities to gain optimal treatment benefits (7, 8). Targeting insomnia and sleep dysfunction may be a promising avenue to improve the quality of treatment for OUD.

Importantly, the relationship between sleep disturbance and OUD outcomes may differ by sex, and although OUD remains more prevalent among men, this gap by sex is rapidly closing (9). Specifically, sleep disorders, especially insomnia, are more prevalent among women than men, and one meta-analysis found that females had a risk ratio of 1.41 of insomnia compared to men (10). Proposed underlying mechanisms for this sleep disparity are numerous, ranging from the role of sex-specific hormones to the impact of gendered social factors that more commonly affect women (11, 12). Therefore, the relationship between sleep and OUD is likely multifaceted with interactions with sex and other biopsychosocial factors (8, 9).

Regarding treatments for insomnia, defined as difficulty initiating or maintaining sleep, current options include pharmacotherapy and behavioral approaches. In the general population, common prescription medications that treat insomnia include benzodiazepines, z-drugs, sedating anti-depressants, and other sedating agents, such as anti-epilepsy medications or atypical antipsychotics (13). However, such medications, particularly benzodiazepines, carry a potential for misuse and respiratory depression in populations with OUD. Additionally, people using substances have historically been excluded from insomnia pharmacotherapy trials, leading to a dearth of evidence on their efficacy in this patient population. Despite these risks and limited understanding of the role insomnia pharmacotherapies could play in people in MOUD treatment, prescribing rates are alarmingly high, especially for females (14). A recent study of multi-state insurance claims found that over 70% of OUD patients with insomnia received benzodiazepine prescriptions during the 60 days following buprenorphine initiation; after adjusting for covariates, female sex remained associated with a greater risk of benzodiazepine prescriptions than male sex (14).

Cognitive behavioral therapy for insomnia (CBTi) is currently the frontline evidence-based behavioral treatment for insomnia (15). CBTi, a multi-component approach covering topics such as cognitive restructuring, stimulus control, sleep restriction, and relaxation, has demonstrated efficacy in the general population as well as in clinical populations when adapted to patient's needs (1619). However, patients' beliefs about sleep problems and practical barriers (e.g., time constraints, work schedules, childcare) can interfere with treatment success (20). Among people with OUD who have more unique barriers to care, there is limited research on CBTi's efficacy. CBTi has demonstrated improvements in sleep primarily among patients with alcohol use disorder (21, 22). To our knowledge, only a single published clinical trial has investigated CBTi among people with OUD; participants included men receiving methadone in Iran, and small improvements in subjective sleep quality were reported (23). Thus, the utility of CBTi as an adjunct to MOUD with buprenorphine for women with comorbid insomnia and OUD is unknown.

Given the complexities lying at the intersection of OUD, sleep, sex, and social determinants of health, it is imperative that insomnia interventions for this patient population are personalized to individuals' biopsychosocial profiles. Further, the unique factors affecting the ability of this population to utilize current medication and behavioral approaches highlights the need for tailored, patient-centered interventions in this domain. Patient insights into what types of interventions are helpful for them, and reasons why, are critical to developing interventions and optimizing their chances of success. However, there is a dearth of research of patient perspectives on sleep interventions for women receiving MOUD. Thus, we conducted an exploratory study to address this gap in the literature and begin to answer the question “what types of sleep interventions would be helpful and usable for women receiving MOUD?” Specifically, the objectives of this study were to (1) describe past experiences and beliefs about sleep and sleep interventions (pharmacotherapy and behavioral), and (2) investigate patient preferences and acceptability of sleep interventions among a sample of women with insomnia receiving buprenorphine for OUD.

Materials and methods

Setting and design

This study used a mixed-methods exploratory design to investigate sleep from the perspective of women in recovery from OUD in an outpatient addiction treatment clinic. The outpatient treatment clinic is affiliated with a large academic medical center in a Southern Medicaid-expanded state, which serves as a safety net for the region and treats predominately individuals with low incomes, with many identifying as a minoritized race or ethnicity. The treatment center prioritizes a low-threshold, harm reduction approach, meaning that established patients with recurrence of substance use are not exited from treatment but instead first provided with increased wrap-around support and referral to a higher level of care. Patients in the program are at various stages of recovery and utilize different combinations of services available at the clinic based upon their needs.

Participants

A research assistant approached patients in the clinic, confirmed eligibility, and invited eligible patients to participate in the study. Patients were pre-identified using a limited medical record review. Study inclusion criteria included the following: OUD diagnosis (24) female sex, stabilized on buprenorphine for at least 6 weeks, aged 18–45, and not pregnant or within 6 weeks postpartum. Exclusion criteria were severe psychosis and non-English-speaking. The Institutional Review Board (IRB) approved all the study components, and informed consent was obtained from all study participants (N = 61). Quantitative data were collected via medical record abstraction and an electronic survey, completed either in-person on a provided tablet or remotely on personal electronic device. For current study quantitative analyses, only those who endorsed clinically significant insomnia symptoms were included (n = 39). Additionally, those participants who endorsed clinically significant insomnia symptoms were eligible to provide qualitative data by participating in semi-structured interviews. A subsample (n = 11) of those with insomnia symptoms completed the interview for the current study.

Measures

Quantitative

Survey demographic items included gender, age, race, employment, education, marital status, and living arrangement. Psychosocial items assessing food, utility, and housing insecurity, healthcare access, and intimate partner violence (IPV) were asked in reference to the past 12 months. Specifically, participants were asked “In the last 12 months, did you ever eat less than you felt you should because there wasn't enough money for food?” and “Are you worried that in the next 2 months, you may not have stable housing?”, to ascertain food and housing insecurity, respectively. Transportation and childcare barriers were assessed using the questions, ‘In the last 12 months, have you ever had to go without healthcare because you didn't have a way to get there?” and “Do problems getting childcare make it difficult for you to work or study?”

The Dysfunctional Beliefs and Attitudes about Sleep (DBAS) Short Form was used to evaluate negative sleep cognitions (25). The DBAS is a 16-item measure that uses a 10-point Likert scale (1- strongly disagree to 10- strongly agree); item scores are averaged for a mean total score ranging from 0 to 10, with higher scores indicating higher endorsement of negative sleep-related cognitions. In addition, the Insomnia Severity Index (ISI) was used to assess insomnia symptoms (26). The ISI is a 7-item measure that uses a 5-point Likert scale (0- none to 4- very severe); items are summed for a total score ranging from 0 to 28, with higher scores indicating higher levels of insomnia symptomatology. Cut-offs of ≥10 were used to identify clinically significant insomnia (26).

The General Anxiety Disorder-7 (GAD-7) was used to assess current symptoms of anxiety. The GAD-7 is a 7-item measure that uses a 4-point Likert scale (0- not at all to 3- nearly every day) in response to questions about frequency of anxiety symptomatology in the past 2 weeks. Item scores are summed for a total score ranging from 0 to 21, with higher scores indicating higher levels of anxiety. Scores ≥10 were considered a positive screen, indicative of clinically significant symptoms of anxiety (27).

The Patient Health Questionnaire-9 (PHQ-9) was used to assess current symptoms of depression. The PHQ-9 is a 9-item measure that uses a 4-point Likert scale (0- not at all to 3- nearly every day) in response to questions about frequency of depression symptomatology in the past 2 weeks. Item scores are summed for a total score ranging from 0 to 27, with higher scores indicating higher levels of depression. Scores ≥10 were considered a positive screen, indicative of clinically significant symptoms of depression (28).

Qualitative

A multidisciplinary team (addiction physician, psychologist, sleep expert) generated the interview guide, which utilized open ended questions to explore patient experiences with and preferences for sleep treatments, adapted from the guide used by Rottapel and colleagues (18). Women responded to questions about familiarity with sleep medications and behavioral treatments, and their experiences with such strategies. During the interview, the research coordinator shared a list of CBT-I strategies around sleep hygiene, stimulus control, and cognitive restructuring, and explored experiences and anticipated challenges with implementing such strategies. Finally, women were asked to think about a tailored sleep health program and respond about barriers and facilitators to participating in such a program. Participants were compensated $15 for their time.

All participants completed interviews using Zoom, a virtual conferencing platform, or in-person in a private office. Two study team members conducted the interviews, with the research coordinator administering the interview and a research assistant taking notes during interviews. Interviews were audio-recorded and lasted 30–60 min. The interviews were transcribed using Zoom transcription software, with the research assistant listening to the transcript and checking the Zoom-automated transcript for fidelity and editing as needed for clarity.

Data management and analysis

Descriptive statistics were generated for demographic, clinical, and psychosocial characteristics as well as self-reported sleep attitudes for the sample with clinically meaningful insomnia symptoms and the qualitative sub-sample.

We utilized the concept of information power, which posits that when powerful data are obtained from each individual participant, then a small sample size may be adequate. Interviews were conducted until data saturation was reached and information redundancy occurred, meaning when new interviews were being conducted no new information was obtained (29, 30).

The interview data were analyzed using a qualitative content analysis approach. This approach allowed for participants' data to provide a comprehensive description of their individual experiences, facilitating a greater understanding of the importance of and beliefs about sleep and sleep interventions for women in treatment for OUD. The qualitative content analysis method facilitated the determination of themes related to the participants' experiences.

The analysis process consisted of several steps. Once interviews from Zoom were transcribed and finalized in Microsoft Word, the analysis team [PI (CEM), research coordinator (ME), and 3 research assistants (CL, SC, SK)] individually reviewed each transcript line by line. The same authors then re-read the transcripts and assigned codes to key concepts that arose from the data. The team met on Zoom to discuss topics that emerged from the codes and, using an inductive process, created a category code list to organize the qualitative data (31). Through group consensus, the group condensed the list into the most salient codes. Finally, an iterative process was then used to group codes and finalize themes and subthemes. The authors identified quotes to highlight themes.

Results

Quantitative

Thirty-nine participants (63.9% of the total study sample) endorsed clinically significant insomnia symptoms, of which 11 participated in a qualitative interview (Table 1). Demographic and clinical characteristics of the qualitative subsample generally reflected those of the larger sample of study participants with clinically elevated levels of insomnia symptoms. Among the 11 participants who completed the qualitative interview, 9 (81.8%) of participants were white, and 2 (18.2%) were Black. The mean age of the qualitative participants was 35.2 (SD = 5.9) years. Five participants (45.5%) indicated that they were currently using medication for sleep, and 2 participants (18.2%) indicated currently receiving therapy for sleep. The average length of time in OUD treatment was 24 months (range: 75–60 months). The most common substances participants reported past 28-day use were for nicotine (n = 7) and cannabis (n = 5).

TABLE 1
www.frontiersin.org

Table 1. Sociodemographic characteristics of participants.

Participants commonly endorsed challenges with social determinants of health (Table 1). Almost one half of participants endorsed food and housing insecurity, and approximately one third endorsed transportation and childcare barriers. In addition, approximately one fifth of participants indicated challenges affording healthcare.

Participants commonly endorsed negative sleep-related cognitions on the DBAS. Levels of such cognitions were similar between the overall sample of participants clinically elevated levels of insomnia symptoms (M = 5.9, SD = 1.1) and the qualitative sub-sample (M = 6.4, SD = 1.1). Many qualitative participants endorsed cognitions about poor sleep interfering with their daily functioning and needing to “catch up” on sleep when they do not get the proper amount. The most highly endorsed cognition was “I need 8 h of sleep to feel refreshed and function well the next day” (Figure 1). The least commonly endorsed cognition amongst qualitative participants was “In order to be alert and function well during the day, I am better off taking a sleeping pill rather than having a poor nights' sleep”.

FIGURE 1
www.frontiersin.org

Figure 1. Negative Sleep-Related Cognitions of Participants.

Qualitative

Four themes emerged from the interviews: (1) positive and negative experiences with sleep treatments, (2) preferences for medications to improve sleep while in OUD recovery, (3) challenges to employing non-pharmacological strategies intended to improve sleep, and (4) preferences for therapy intended to address sleep for individuals in OUD treatment. Table 2 provides a list of the themes, sub-themes within each respective theme, and a representative quote.

TABLE 2
www.frontiersin.org

Table 2. Qualitative themes, codes and quotes.

Theme 1: Prior experiences with sleep treatments

Generally, participants expressed both positive and negative experiences with treatments for sleep. The most commonly mentioned medications were zolpidem (n = 4), trazodone (n = 4), and quetiapine (n = 3). Some medications, such as zolpidem and hydroxyzine were explicitly prescribed to participants to assist with sleep. However, participants also shared experiences with over-the-counter medications, such as “Tylenol PM” and melatonin supplements, to help with sleep. Participants had mixed experiences with medication and impact on sleep. For example, two participants indicated that trazodone helped with sleep while two others noted it was not particularly helpful with sleep.

Participants also shared experiences with behavioral strategies. They were familiar with behavioral strategies for sleep and reported being familiar with sleep hygiene strategies such as reducing electronic usage before bed and limiting screens (e.g., television) in the bedroom (n = 5), meditation and mindfulness (n = 4), and stimulus control, limiting the bed only to sleep (n = 2). Participants reported that behavioral and medication treatments are often siloed and delivered by different healthcare providers and entities, making the implementation of such strategies more challenging.

Theme 2: Preferences for medications to improve sleep while in OUD recovery

All participants (n = 11) expressed that they would take a medication to improve sleep if it was prescribed by their health care provider. They noted a preference for a safe medication to improve sleep quality and quantity, particularly to lengthen the duration of sleep. Participants expressed the desire for a medication to have minimal side effects, such as grogginess the following morning, and improve irritability, as lack of sleep would often affect their mood negatively. However, because most of the sample were caregivers for children or family members (n = 10), they reported that the medication could not “knock them out” or be too sedating that they would not be able to give care in the middle of the night. In addition, participants expressed that the medication could not be associated with risk of dependence. Participants shared that recovery was important to them, and any medication that would interfere with their recovery was undesirable.

Theme 3: Challenges to employing non-pharmacologic strategies for sleep while in OUD recovery

Most participants had heard of non-pharmacologic sleep strategies. However, participants expressed that these strategies, among others, are hard to employ for various reasons. For example, the majority of participants expressed regular consumption of caffeine and nicotine, two substances that negatively impact sleep. Participants also shared that their physical environments would make implementation of such strategies difficult, as they reported challenges with sharing small spaces with multiple people, or sleeping in different areas of the house so that they could be close to family members to give care.

Participants also expressed that negative cognitions that occur at night impact the ability to engage in behavioral strategies. For example, several participants noted that “stinking thinking”, a concept referring to negative cognitive distortions about ability to maintain recovery as well as negative memories associated with active addiction are common at night and while trying to initiate sleep, worsening insomnia symptoms.

Theme 4: Preferences for non-pharmacologic sleep treatment delivery method for individuals in OUD treatment

Participants noted pros and cons of both telehealth and in-person delivery options for therapy to address issues with sleep. Most participants noted that they appreciated telehealth options, particularly due to the convenience of being able to do sessions from home. However, some participants also reflected that telehealth has challenges, specifically lack of phone or internet connection required to complete telehealth sessions depending on their geographic location. Participants expressed that in-person sessions would keep them accountable to the process of behavioral sleep treatment, and that accountability is a factor in recovery as well. Conversely, participants also shared that attending in-person sessions can be challenging depending on childcare or transportation needs and reflected that flexibility of having both virtual and in-person options may help address this.

Discussion

This mixed-methods study explored past experiences and beliefs about treatments (pharmacologic and behavioral) for sleep disturbances as well as preferences and acceptability of sleep interventions among women with comorbid insomnia receiving buprenorphine in outpatient OUD treatment. We utilized quantitative data to describe the sample and supplemented such data with rich qualitative data from in-depth interviews.

Women receiving MOUD described both high quality and appropriate quantity of sleep were important to their daily functioning and their recovery. They highlighted varying impacts of their experiences with medication and behavioral therapy for sleep. However, existing modalities of sleep interventions are largely insufficient in this population for a variety of reasons. For instance, although the women in this sample reported that they would take a medication if prescribed by their provider, most of our sample would rather cope with a poor night of sleep than take a “sleeping pill.” Medications perceived to carry the risk of dependence could compromise their recovery and are undesirable, precluding several sleep medications commonly prescribed for insomnia (32). Clearly many existing pharmacological interventions for insomnia may not be appropriate for this population due to their OUD and associated experiences and recovery goals. Overall, these preferences expressed by women in our sample are important to consider as new pharmacologic insomnia interventions are generated and evaluated in the MOUD patient population.

Women also reported that they would not want a medication that was too sedating, as it would impact their ability to take care of family members. Participants commonly reported that caregiving was a barrier to sleep. Similarly, Rottapel et al. found in their qualitative exploration of barriers to sleep among a community sample that caregiving was cited as the most common barrier. Parents valued sleep, yet the demands of childcare negatively impact sleep (2019). Women experience caregiver strain more than men, which may impact their ability to address their own healthcare needs such as quality sleep.

The participants also detailed how social determinants of health can impact successful participation in pharmacologic and non-pharmacological sleep interventions by MOUD patients (conceptualized in Figure 2). For example, transportation barriers were endorsed in both quantitative and qualitative results. Most of the women in our sample indicated that they often had transportation issues that would impede them from being able to attend regular in-person therapy sessions, but also noted internet and phone connectivity issues as barriers to telehealth sessions. In addition, women often noted that in-person sessions help with accountability to the therapeutic process, with accountability being a major component of recovery. Other social determinants of health commonly reported that may affect sleep and ability to participate in in-person interventions, included housing insecurity and challenges obtaining childcare. Thus, the myriad of factors that can impact ability to participate in non-pharmacological treatment necessitate flexible and adaptable modalities of sleep interventions, emphasizing the importance of individualizing treatments for MOUD patients.

FIGURE 2
www.frontiersin.org

Figure 2. Insomnia in context.

Targeted sleep treatment may have impacts not only on insomnia, but also on co-morbid mental health conditions. Almost half of the qualitative sample endorsed clinically significant anxiety and over half the sample endorsed clinically significant depression. Further, participants reflected on their experiences with negative memories associated with active addiction, indicating a need to co-treat broader mental health concerns such as PTSD, anxiety, and depression. Insomnia can have bi-directional relationships with anxiety and depression, and thus treatment of insomnia might alleviate mental health symptoms (33). Thus, targeting insomnia in OUD treatment may be an avenue to simultaneously target multiple underlying mechanisms (e.g., negative emotionality, impulsivity) contributing to MOUD outcomes, an area in need of further investigation.

Clinical and research implications

Insomnia is prevalent among women receiving MOUD. It impacts quality of life and OUD recovery. Current evidence-based treatments are ill-suited for this population. Findings highlight the need to provide holistic, flexible, integrated insomnia and mental health treatment with addiction treatment. Future studies should address development, implementation, and evaluation of tailored sleep treatments among people with OUD that account for the unique social determinants of health and other sleep-related considerations that affect this population.

Limitations

We only included women currently in treatment, receiving MOUD at a single outpatient addiction treatment clinic in the U.S., which limits generalizability of findings to other populations or settings. However, our selective sample is also a strength, as our findings are pertinent to an increasingly more prevalent patient population in the overdose crisis. Our findings shed light on sleep in this population, allowing us to learn from their experiences to expand the evidence base to improve sleep treatment for women with OUD.

Conclusion

Clinically elevated insomnia symptoms were highly prevalent among women with OUD. Findings suggest delivery of existing modalities of sleep interventions are insufficient for this population. This research highlights the need for evidence-based, tailored treatment options that account for the unique social determinants of health and other sleep-related considerations that affect this population. Incorporating patient preferences and input through a sex and gender informed lens into the development, implementation, and evaluation of sleep treatments among people with OUD has the potential to make an immediate and significant positive impact on this population.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving humans were approved by Virginia Commonwealth University. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.

Author contributions

ME: data collection, analysis, and writing and editing. AP-A: review and editing. CL, SC, and SK: analysis. SV: conceptualization and data collection. JD: conceptualization, design, and review and editing. AH and AW: review and editing. CM: conceptualization, methodology, supervision, writing, review, and funding acquisition. All authors contributed to the article and approved the submitted version.

Funding

This study was supported by the NIDA award no. T32DA007027 (ME), NIDA award no. K23DA053507 (PI: CM), and the National Center for Advancing Translational Sciences UL1TR002649 (Virginia Commonwealth University Wright Center).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Gomes T, Tadrous M, Mamdani MM, Paterson JM, Juurlink DN. The burden of opioid-related mortality in the United States. JAMA Network Open. (2018) 1:e180217. doi: 10.1001/jamanetworkopen.2018.0217

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Woolf SH, Schoomaker H. Life expectancy and mortality rates in the United States, 1959-2017. JAMA. (2019) 322:1996. doi: 10.1001/jama.2019.16932

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Wakeman SE, Larochelle MR, Ameli O, Chaisson CE, McPheeters JT, Crown WH, et al. Comparative effectiveness of different treatment pathways for opioid use disorder. JAMA Network Open. (2020) 3:e1920622. doi: 10.1001/jamanetworkopen.2019.20622

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Greenwald MK, Moses TEH, Roehrs TA. At the intersection of sleep deficiency and opioid use: mechanisms and therapeutic opportunities. Transl Res. (2021) 234:58–73. doi: 10.1016/j.trsl.2021.03.006

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Huhn AS, Finan PH. Sleep disturbance as a therapeutic target to improve opioid use disorder treatment. Exp Clin Psychopharmacol. (2022) 30:1024–35. doi: 10.1037/pha0000477

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Wilkerson AK, McRae-Clark AL. A review of sleep disturbance in adults prescribed medications for opioid use disorder: potential treatment targets for a highly prevalent, chronic problem. Sleep Med. (2021) 84:142–53. doi: 10.1016/j.sleep.2021.05.021

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Dunn KE, Finan PH, Andrew Tompkins D, Strain EC. Frequency and correlates of sleep disturbance in methadone and buprenorphine-maintained patients. Addict Behav. (2018) 76:8–14. doi: 10.1016/j.addbeh.2017.07.016

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Valentino RJ, Volkow ND. Drugs, sleep, and the addicted brain. Neuropsychopharmacology. (2020) 45:3–5. doi: 10.1038/s41386-019-0465-x

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Martin CE, Dzierzewski JM, Keyser-Marcus L, Donovan EK, Ramey T, Svikis DS, et al. Sex specific sleep parameters among people with substance use disorder. Front Psychiatry. (2022) 13:905332. doi: 10.3389/fpsyt.2022.905332

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Zhang B, Wing Y-K. Sex differences in insomnia: a meta-analysis. Sleep. (2006) 29:85–93. doi: 10.1093/sleep/29.1.85

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Brown AMC, Gervais NJ. Role of ovarian hormones in the modulation of sleep in females across the adult lifespan. Endocrinology. (2020) 161:bqaa128. doi: 10.1210/endocr/bqaa128

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Jackson CL, Powell-Wiley TM, Gaston SA, Andrews MR, Tamura K, Ramos A. Racial/ethnic disparities in sleep health and potential interventions among women in the United States. J Womens Health. (2020) 29:435–42. doi: 10.1089/jwh.2020.8329

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Lie JD, Tu KN, Shen DD, Wong BM. Pharmacological treatment of insomnia. P T Peer-Rev J Formul Manag. (2015) 40:759–71.

Google Scholar

14. Martin CE, Patel H, Dzierewski JM, Moeller FG, Bierut LJ, Grucza RA, et al. Benzodiazepine, Z-drug and sleep medication prescriptions in male and female people with opioid use disorder on buprenorphine and comorbid insomnia: an analysis of multi-state insurance claims. Sleep. (2023) 46:zsad083. doi: 10.1093/sleep/zsad083

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Qaseem A Kansagara D Forciea MACooke M Denberg TD for for the Clinical Guidelines Committee of the American College of Physicians. Management of chronic insomnia disorder in adults: a clinical practice guideline from the American College of physicians. Annals Int Med. (2016) 165:125. doi: 10.7326/M15-2175

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Cheng P, Luik AI, Fellman-Couture C, Peterson E, Joseph CLM, Tallent G, et al. Efficacy of digital CBT for insomnia to reduce depression across demographic groups: a randomized trial. Psychol Med. (2019) 49:491–500. doi: 10.1017/S0033291718001113

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Dzierzewski JM, Martin JL, Fung CH, Song Y, Fiorentino L, Jouldjian S, et al. CBT for late-life insomnia and the accuracy of sleep and wake perceptions: results from a randomized-controlled trial. J Sleep Res. (2019) 28:e12809. doi: 10.1111/jsr.12809

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Rottapel RE, Zhou ES, Spadola CE, Clark CR, Kontos EZ, Laver K, et al. Adapting sleep hygiene for community interventions: a qualitative investigation of sleep hygiene behaviors among racially/ethnically diverse, low-income adults. Sleep Health. (2020) 6:205–13. doi: 10.1016/j.sleh.2019.12.009

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Zhou ES, Ritterband LM, Bethea TN, Robles YP, Heeren TC, Rosenberg L. Effect of culturally tailored, internet-delivered cognitive behavioral therapy for insomnia in black women: a randomized clinical trial. JAMA Psychiatry. (2022) 79:538–49. doi: 10.1001/jamapsychiatry.2022.0653

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Koffel E, Bramoweth AD, Ulmer CS. Increasing access to and utilization of cognitive behavioral therapy for insomnia (CBT-I): a narrative review. J Gen Intern Med. (2018) 33:955–62. doi: 10.1007/s11606-018-4390-1

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Chakravorty S, Morales KH, Arnedt JT, Perlis ML, Oslin DW, Findley JC, et al. Cognitive behavioral therapy for insomnia in alcohol-dependent veterans: a randomized, controlled pilot study. Alcohol Clin Exp Res. (2019) 43:1244–53. doi: 10.1111/acer.14030

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Miller MB, Donahue ML, Carey KB, Scott-Sheldon LAJ. Insomnia treatment in the context of alcohol use disorder: a systematic review and meta-analysis. Drug Alcohol Depend. (2017) 181:200–7. doi: 10.1016/j.drugalcdep.2017.09.029

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Robabeh S, Jafar MM, Sharareh H, Maryam HR, Masoumeh E. The effect of cognitive behavior therapy in insomnia due to methadone maintenance therapy: a randomized clinical trial. Iran J Med Sci. (2015) 40:396–403.

PubMed Abstract | Google Scholar

24. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 5th ed. Virginia: American Psychiatric Association (2013).

Google Scholar

25. Morin CM, Vallières A, Ivers H. Dysfunctional beliefs and attitudes about sleep (DBAS): validation of a brief version (DBAS-16). Sleep. (2007) 30:1547–54. doi: 10.1093/sleep/30.11.1547

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Morin CM, Belleville G, Bélanger L, Ivers H. The Insomnia Severity Index: Psychometric indicators to detect insomnia cases and evaluate treatment response. Sleep. (2011) 34:601–8. doi: 10.1093/sleep/34.5.601

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Spitzer RL, Kroenke K, Williams JBW, Löwe B. A brief measure for assessing generalized anxiety disorder: the GAD-7. Arch Intern Med. (2006) 166:1092–7. doi: 10.1001/archinte.166.10.1092

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. (2001) 16:606–13. doi: 10.1046/j.1525-1497.2001.016009606.x

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Morse JM. The significance of saturation. Qual Health Res. (1995) 5:147–9. doi: 10.1177/104973239500500201

CrossRef Full Text | Google Scholar

30. Vasileiou K, Barnett J, Thorpe S, Young T. Characterising and justifying sample size sufficiency in interview-based studies: systematic analysis of qualitative health research over a 15-year period. BMC Med Res Methodol. (2018) 18:148. doi: 10.1186/s12874-018-0594-7

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Thomas DR. A general inductive approach for analyzing qualitative evaluation data. American Journal of Evaluation. (2006) 27:237–46. doi: 10.1177/1098214005283748

CrossRef Full Text | Google Scholar

32. Grandner M, Ahuja A, Meijer P, Büsser A, McCall W, Lettieri C. 0460 First-line treatment patterns in patients with insomnia: a large-scale, real-world cohort study. Sleep. (2022) 45(Suppl. 1):A204. doi: 10.1093/sleep/zsac079.457

CrossRef Full Text | Google Scholar

33. Khurshid KA. Comorbid insomnia and psychiatric disorders: an update. Innov Clin Neurosci. (2018) 15:28–2.

PubMed Abstract | Google Scholar

Keywords: insomnia, sleep, buprenorphine, opioid use disorder, substance use disorder treatment

Citation: Eglovitch M, Parlier-Ahmad AB, Legge C, Chithranjan S, Kolli S, Violante S, Dzierzewski JM, Huhn AS, Wilkerson A and Martin CE (2023) Patient reported preferences for sleep interventions among women receiving buprenorphine for opioid use disorder. Front. Psychiatry 14:1244156. doi: 10.3389/fpsyt.2023.1244156

Received: 21 June 2023; Accepted: 29 August 2023;
Published: 14 September 2023.

Edited by:

Helena Martynowicz, Wroclaw Medical University, Poland

Reviewed by:

Vahid Farnia, Kermanshah University of Medical Sciences, Iran
Emily E. Hartwell, United States Department of Veterans Affairs, United States

Copyright © 2023 Eglovitch, Parlier-Ahmad, Legge, Chithranjan, Kolli, Violante, Dzierzewski, Huhn, Wilkerson and Martin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Michelle Eglovitch, eglovitchms@vcu.edu

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.