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Mechanisms of Change in Cognitive Behavioral Therapy for Insomnia (CBTi)

Recruiting
50 - 65 years of age
Both
Phase N/A

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Overview

The purpose of this study is to investigate the mechanisms of change in Cognitive Behavioral Therapy for insomnia (CBTi) in a sample of adults aged 50-65. This study aims to evaluate the pre-post treatment change in sleep, circadian rhythms, biomarkers, cognitive performance, and structural and functional magnetic resonance imaging scans (MRI).

Description

Baseline Part 1:

  • Online demographic and contact information
  • Schedule Baseline Part 2 with the investigators via online link
  • 1 week of daily sleep diaries

Baseline Part 2:

  • Internet-based interview with the investigators to confirm study eligibility requirements
  • Online self-report questionnaires
  • 2 weeks of daily sleep diaries
  • 2 weeks of sleep/wake assessment wearing a watch-like activity monitor (Actiwatch)

Objective Baseline:

  • Single-night, diagnostic in-home sleep study, including and the following equipment:
  • Adhesive patch which will adhere to the arm
  • Sensor belts worn around the chest, fitted with nasal canula, pulse oximeter, and 3 electrodes which will adhere to the back of the neck and behind each ear
  • Next-day appointment:
  • Neuropsychological assessment
  • Structural and functional magnetic resonance imaging scan (MRI)
  • Non-invasive blood pressure readings
  • Low-volume Blood draw (used to obtain genetic biomarkers)
  • Removal of adhesive patch
  • Next-day evening (2-nights):
  • Consumable capsule
  • Sensor belt worn around the chest/abdomen Random Assignment: If it is determined the participant is eligible for the study, participants will be randomly assigned to one of the treatment groups (in-person, telehealth or internet delivered) or asked to wait to start treatment.

Treatment Phase I:

  • Participants will complete up to 12 weeks of insomnia treatment or wait for treatment ("waitlist") 12-Week Post-treatment Part 1:
  • Complete 2 weeks of an online daily sleep diary and actigraphy
  • Complete online self-report questionnaires

Objective 12-Week Post-treatment:

• Repeat "Objective Baseline" outlined above

Treatment Phase II (WLC):

  • Treatment will start for participants who had been assigned to the waitlist condition 3-Month Follow-Up:
  • Complete online self-report questionnaires

Eligibility

Inclusion Criteria:

  • Aged 50-65
  • Normal hearing with or without hearing aids
  • Ability to speak and read English and ability to give informed consent
  • Possession of a computer with video and audio capabilities
  • Meets DSM-5 Criteria for Insomnia Disorder
  • Internet speed sufficient for participating in teletherapy (e.g., Zoom Health) or SHUTi (for iCBTi group)
  • MoCA scores ≥24 will be deemed normal cognitive status and considered eligible for study participation and/or assessed by the ability to comprehend the baseline screening questionnaires
  • Willing to refrain from new external behavioral health or medication treatment for issues pertaining to sleep during participation in the study
  • Indication that the individual plans to be in the area for the 6 months following the first baseline assessment

Exclusion Criteria:

  • Failure to meet the above "inclusion criteria"
  • Current circadian rhythm disorder, sleep deprivation, or hypersomnia and related sleep disorders (assessed with clinical interview and/or self-report) as CBTi has not been validated in these populations. Verified by self-report and/or clinical interview (SCISD-R)
  • Untreated sleep disordered breathing (e.g., obstructive sleep apnea) assessed by self-report, clinical interview, and/or diagnostic sleep study (i.e., baseline sleep study PSG)
  • Failing to meet criteria for MRI scan (e.g., having metallic implants); see Pre-screen MRI Checklist for full list of exclusions for MRI scans.
  • Fear/phobia of needles (conflict with blood draw) and/or small spaces (conflict with MRI scanner)
  • Current suicide risk meriting crisis intervention as assessed by the Patient Health Questionnaire (PHQ-9) and/or disclosure of serious suicidal ideation
  • Pregnancy (self-report, proposed instruments and treatments have not been validated in this population)
  • Sleep efficiency > 85%, assessed by the sleep diary
  • Serious mental health diagnosis (e.g., bipolar disorder or psychosis) assessed by structured interview (M.I.N.I.)
  • Currently engaged in evidence-based psychotherapy for Insomnia (i.e., Cognitive Behavioral Therapy) by self-report
  • Failure to follow protocol (e.g., consistent "no show" for appointments, answering questionnaires dishonestly, refusal to complete more than 2 assessments [e.g., fMRI and Neuropsych])

Study details

Sleep Initiation and Maintenance Disorders

NCT05226585

University of Arizona

15 May 2024

Step 1 Get in touch with the nearest study center
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