Clinical trial Recruiting at 1 site Interventional Ages 50 and up

I-SLEPT: Integrated Sleep and Life Engagement for Transitions

Official title: I-SLEPT: Integrated Sleep and Life Engagement Program for Transitions

Run by VA Office of Research and Development · NCT07317336 · Data updated 2026-11-12

This project tests a sleep and life-engagement program designed to help Veterans re-adjust after hospital discharge.

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Quick facts

Study typeInterventional
Ages50 Years and up
SexAll
Enrollment60 (estimated)
SponsorVA Office of Research and Development
Federal
Locations1 site (Boston, Massachusetts)
StatusRecruiting
StartedJune 22, 2026
Main results expectedMarch 31, 2031
Study endsMarch 31, 2031
Registry record updatedOctober 23, 2026
Trial IDNCT07317336 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are Veterans aged 50+ who are discharged home from VA Boston acute care or subacute rehab units, are English-speaking, have adequate cognitive status, and report sleep or life-engagement challenges.

Probably not a fit

Patients who are discharged to long-term care, have severe cognitive impairment, or have conditions that markedly hinder sleep or daily participation may receive limited or no benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study develops and tests a sleep-health and life-engagement intervention called I-SLEPT for Veterans transitioning from VA acute hospitalization or subacute rehabilitation to home. It uses a phased, single-arm approach starting with interviews and surveys to inform the program, followed by a preliminary trial and a proof-of-concept phase to assess sleep health, participation in meaningful activities, and acceptability. The program aims to stabilize sleep and maximize participation in daily activities during a vulnerable recovery period. Outcomes will inform potential expansion to additional transition points and broader implementation by multidisciplinary staff.

Why it matters

Potential benefit: If successful, the program could improve sleep quality and daily functioning during post-discharge recovery for Veterans.

How similar studies have gone: Previous studies in transitional care have shown that sleep-focused and engagement-enhancing strategies can improve function, though this specific integrated program for Veterans is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Admitted to and discharged from VA Boston acute care units OR Community Living Center subacute rehabilitation unit
* English-speaking
* Discharged to a home setting
* Has capacity and does not have severe cognitive impairment
* Obtains a score \>= 8 on the Brief Interview for Mental Status (BIMS)
* Endorses at least 2 items as "Rarely/Never" or "Sometimes" on the RuSATED measure AND/OR endorses they are achieving their goals at a "much worse" or "a little worse" level on the What Matters Most Tool

Exclusion Criteria:

* Discharged from Long-Term Care, Hospice and Palliative Care, or Spinal Cord Injury bed specialty
* Discharged from intensive care units
* Moderate to severe dementia diagnosis, delirium, or active psychosis
* Healthcare proxy is activated in electronic health record
* A diagnosis of a disorder of hypersomnolence, non-REM parasomnia, or Nightmare Disorder as indicated in electronic health record
* High acute risk for suicide

Where it's running

  • VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
    Boston, Massachusetts, United States
    Recruiting

Study contacts

  • Principal investigator: Julia T Boyle, PsyD — VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
  • Study coordinator: Julia T Boyle, PsyD
  • Email: julia.boyle@va.gov
  • Phone: (617) 963-6391

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.