Digital sleep program for older adults having joint surgery, studying insomnia and brain health
Tests a phone-based insomnia program in older adults having major joint surgery.
Key facts
- Who runs it
- Massachusetts General Hospital
- Where
- Boston, United StatesSee the site
- Trial code
- Registry title
- Digital Sleep Optimization for Brain Health Outcomes in Older Surgical Patients
- Status
- Recruiting
- People taking part
- 50 people, planned
- Started
- 15 Jan 2025
- Expected to end
- 31 Dec 2026
- Type of study
- Interventional, 2 groupsOne group gets an existing treatment, for comparison.
- Treatments tested
- digital Cognitive Behavioral Therapy for Insomnia (dCBT-I)
- Sleep Health Education
- Record updated
- 14 September 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults aged 65 or older with at least mild insomnia who are scheduled for a planned knee or hip replacement. It tests a sleep therapy phone app with a wrist sleep tracker.
- Age
- 65 years and older
- Sex
- All sexes
- Disease stage
- At least mild insomnia (ISI score of ≥10 on screening). Scheduled for a planned total knee or hip replacement.
- Earlier treatment
- No cognitive behavioral therapy for insomnia (CBT-I) now or in the last 6 months before the study.
Main reasons for not taking part
- Fast-worsening illness or life expectancy under 6 months
- Active psychosis or thoughts of suicide
- Irregular shift work or sleep patterns, or sleep disorders other than insomnia or apnea
- Moderate-severe sleep apnea (apnea/hypopnea index ≥15) without regular CPAP use
- Dementia, or starting, stopping or changing sleep-affecting prescription medicines within 1 month before the study or during it
The registry criteria, word for word
Show all 13 criteriaShow less
Who can take part
- Adults ≥ 65 years old
- Scheduled for an elective orthopedic total joint replacement procedure (knee/hip)
- At least mild insomnia (ISI score of ≥10 on telephone screening or RedCap screening questionnaire)
- Own a smart phone 6. Willingness to use the dCBT-I app and actigraphy
Who cannot take part
- Current or previous CBT-I exposure in the last 6 months prior to the start of the study
- Initiation, discontinuation, or dose change of sleep-affecting prescription medications within 1 month prior to study start or during the intervention period; not excluded if stable sleep-affecting medications in the prior month (by clinical review)
- No surgery within 12 months of consented, eligibility will be reassessed if surgery is delayed by more than 3 months
- Rapidly progressive illnesses/life expectancy <6 months
- Sleep disorders other than insomnia or apnea
- Cognitive impairment (diagnosis of dementia)
- Active psychosis/suicidal ideation
- Irregular shift work/sleep patterns
- Moderate-severe sleep apnea (apnea/hypopnea index ≥15) without CPAP compliance per chart review
Where in United States
- Massachusetts General HospitalBoston, United StatesContact: Lei Gao, MDTaking people
About the trial
What the trial wants to find out
The Sleep Optimization for Brain Health Outcomes in Older Surgical Patients (SLEEP-BOOST) is a pilot randomized, controlled, singled-blinded (participant) trial in major orthopedic joint surgery patients that will build on a previously clinically tested cognitive behavioral therapy for insomnia (CBT-I) mobile application paired with a wearable device (wrist actigraphy).
The 2 groups in the trial
- Digital CBT-ITreatment being tested
Preoperative digital CBT-I with the CBT-I Coach app for up to 4 weekly sessions and postoperative booster sessions at 2 weeks and 1 month after surgery.
Treatment: digital Cognitive Behavioral Therapy for Insomnia (dCBT-I)
- Sleep Health EducationExisting treatment, for comparison
Preoperative sleep health education materials
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- A Pilot Study of Digital Sleep Optimization for Brain Health Outcomes in Older Surgical Patients (SLEEP-BOOST)
- Plain-language title
- Digital sleep program for older adults having joint surgery, studying insomnia and brain healthGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 14 November 2026.
- Publications
- Record updated
- 14 September 2026