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Completed

NCT Number: NCT02887209

A Pragmatic Pilot Study of Cognitive Behavioural Therapy for Insomnia Among People Living With HIV

Insomnia is a problem for approximately 75% of people living with HIV, which is much higher than the 6% to 10% of people with insomnia in the general population. It is currently unknown why the rate of insomnia is so high among people living with HIV, and because of this, they are often excluded from clinical trials examining the usefulness of cognitive behavioural therapy for insomnia (CBT-I), which is recommended as the first-line treatment for insomnia. Insomnia is also associated with poorer immune functioning and lower medication adherence. The purpose of this study is to examine whether CBT-I is useful at reducing insomnia among people living with HIV, and to examine whether this counselling is safe to provide to this population. Other purposes are to explore whether reducing insomnia will lead to improved immune functioning and medication adherence, to collect feedback about people's experiences receiving CBT-I, to examine which psychological and behavioural factors are associated with insomnia severity among people living with HIV.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Psychology, Ryerson University

Toronto, Ontario, M5B 2K3, Canada

About this study

The prevalence of insomnia in the general population ranges from 6% to 10% (American Psychiatric Association, 2013), whereas its estimated prevalence among people living with HIV (PWH) is 73% (Rubinstein & Selwyn, 1998). Cognitive, behavioural, physiological, and psychosocial explanations for this elevated prevalence have been proposed (Taibi, 2013), however, there is a lack of consensus in the literature. Sleep disturbance is associated with disrupted immune functioning at the cellular level (Taylor, Lichstein, & Durrence, 2003), as well as increased risk of contracting infectious diseases (Patel et al., 2012); therefore, insomnia may be particularly problematic for PWH. Cognitive behavioural therapy for insomnia (CBT-I; Edinger & Carney, 2008) is the first-line treatment for insomnia (Qaseem et al., 2016; Schutte-Rodin et al., 2008), and medium to large effect sizes have been reported (Okajima et al., 2011). CBT-I is effective at treating insomnia among individuals with comorbid medical disorders such as chronic pain (Jungquist et al., 2012), fibromyalgia (Martínez et al., 2014), and cancer (Garland et al., 2014). Surprisingly, no study to date has examined the efficacy of CBT-I among PWH. The current study will evaluate the safety, feasibility, acceptability, and effects of CBT-I among 20 PWH using a pragmatic pilot study design. An exit interview will be conducted to elicit participant feedback about the treatment and methods used. Additional cross-sectional analyses will examine predictors of insomnia symptom severity and other sleep-related outcomes among a larger sample (n = 60). This will be the first study to examine the impact of CBT-I among PWH.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years of age or older
  • able to understand and communicate in English
  • capable of providing informed consent
  • presence of insomnia based on screener questionnaire cutoff score ≥ 15 on the Insomnia Severity Index
  • HIV-seropositive
  • willing to provide HIV viral load and CD4 count from blood work within the past two months

Exclusion criteria

  • active suicidal ideation
  • psychotic symptoms
  • unmanaged bipolar disorder
  • presence of a severe alcohol or substance use disorder according to Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 criteria
  • hypnotic dependence
  • presence of any breathing-related sleep disorders (obstructive sleep apnea hypopnea, central sleep apnea, and sleep-related hypoventilation), or circadian rhythm sleep-wake disorders
  • working shift work or frequent time zone travel over the course of the study
  • contingent or inconsistent hypnotic use, or anticipated change in hypnotic medication dose over the course of the study
  • receiving psychotherapy for insomnia or any other mental disorder over the course of the study
  • presence of an AIDS-defining opportunistic infection and/or a CD4 count < 200

Treatment and study plan

CBT-I

Behavioral

Cognitive behavioural therapy for insomnia (CBT-I; Edinger & Carney, 2008) is a standard 4-session cognitive behavioural therapy for insomnia administered biweekly in individual format. The first session involves presenting treatment rationale and introducing a behavioural treatment regimen consisting of a series of sleep habit parameters to follow, and determining a personalized "time in bed" prescription. The second session involves reviewing past-week sleep diary, discussing the role of cognitions in insomnia, and discussing constructive worrying techniques and the use of thought records. The third and fourth sessions are used to assist in adjusting "time in bed" prescriptions, to positively reinforce efforts, and to help problem-solve any problems they might have encountered.

Primary outcomes

  1. Insomnia symptom severity

    Time frame: Two weeks post-treatment

    Insomnia symptom severity is measured using the Insomnia Severity Index (ISI)

Secondary outcomes

  1. CD4+ (cluster of differentiation 4) cell count

    Time frame: Within two months post-treatment

    Obtained via self-report based on blood test results in past 3 months

  2. HIV viral load

    Time frame: Within two months post-treatment

    Obtained via self-report based on blood test results in past 3 months

  3. Combined antiretroviral therapy (cART) medication adherence

    Time frame: Two weeks post-treatment

    Measured using the Self-Rating Scale Item (SRSI) and Simplified Medication Adherence Questionnaire (SMAQ)

  4. Sleep efficiency

    Time frame: Two weeks post-treatment

    Sleep efficiency is the amount of time spent sleeping vs. awake in bed

  5. Total wake time

    Time frame: Two weeks post-treatment

    Total wake time is the total time spent awake between getting into bed at night

Other outcomes

  1. Health-related quality of life

    Time frame: Two weeks post-treatment

    Measured using the Medical Outcomes Study Short-Form Health Survey (SF-36)

  2. Depression symptom severity

    Time frame: Two weeks post-treatment

    Measured using the Centre for Epidemiological Studies in Depression Scale-Revised (CESD-R) and Depression Anxiety Stress Scales (DASS-21)

  3. Treatment acceptability

    Time frame: Immediately post-treatment (final therapy session)

    Measured using the Therapy Evaluation Questionnaire (TEQ)

  4. Intervention safety

    Time frame: Two weeks post-treatment

    Measured via qualitative exit interview, and includes any unwanted or adverse events associated with the intervention

  5. Dysfunctional beliefs about sleep

    Time frame: Two weeks post-treatment

    Measured using the Dysfunctional Beliefs and Attitudes about Sleep Scale (DBAS-16)

  6. Sleep effort

    Time frame: Two weeks post-treatment

    Measured using the Glasgow Sleep Effort Scale (GSES)

  7. Self-efficacy for sleep

    Time frame: Two weeks post-treatment

    Measured using the Self-Efficacy for Sleep Scale (SE-S)

  8. Pre-sleep arousal

    Time frame: Two weeks post-treatment

    Measured using the Pre-Sleep Arousal Scale (PSAS-13)

  9. Fatigue

    Time frame: Two weeks post treatment

    Measured using the Fatigue Severity Scale (FSS)

  10. Anxiety Symptom Severity

    Time frame: Two weeks post treatment

    Measured using the Depression Anxiety Stress Scales (DASS-21)

  11. HIV-Related Fatigue

    Time frame: Two weeks post treatment

    Measured using the HIV-Related Fatigue Scale (HRFS)

Sponsors and collaborators

Lead sponsor

Toronto Metropolitan University

Other

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Sep 2, 2016
Registry last updated
Aug 14, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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