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NCT06758505Recruiting

Rehabilitation Strategies for Social Participation in Chronic Stroke Survivors

Source: ClinicalTrials.gov · Last updated 29 Sept 2026

Brief summary (registry, in English)

The goal of this clinical trial is to test a new rehabilitation program, combining acceptance and commitment therapy with strategy training (ACES), to help people resume social participation after stroke and live in the community. Investigators will also compare the changes in social participation and psychological flexibility from baseline to follow-up at one-month after rehabilitation to see if participants who receive ACES report clinically meaningful improvements (Cohen's d=0.2 or greater) compared to the existing rehabilitation program using strategy training alone (START). Participants will: * complete testing to see if they are eligible for the study. If qualified, complete testing to understand how the stroke has affected their daily life * be randomized to receive either ACES or START rehabilitation program for 10 sessions at their home * repeat part of the tests at the end of the intervention and one month after

Status (registry)
Recruiting
Study type
Interventional
Enrollment
54 (estimated)
First submitted
18 Dec 2024
Start date
29 Sept 2025
Primary completion date
Jun 2027
Lead sponsor
University of Pittsburgh
Diseases
Stroke
NCT number
NCT06758505

What you commit to

  • Study type: Interventional
  • Planned participants: 54
  • From 29 Sept 2025 to the primary completion date, Jun 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • progressive neurological diagnosis (e.g., dementia, Parkinson's disease, multiple sclerosis, or brain tumor) reported by participants or proxy,
  • currently undergoing stroke rehabilitation or mental health intervention (but participation in maintenance sessions, self-help groups, or couples therapy is permitted),
  • major depressive disorder, indicated by PRIME-MD, unless undergoing treatment for at least 4 weeks and are released to participate by their physician or counselor
  • bipolar or psychotic disorder, indicated by PRIME-MD, or
  • substance use disorder within 3 months, indicated by Mini-International Neuropsychiatric Interview

Other

  • inability to provide written informed consent,
  • severe aphasia (score 0 or 1 on the Boston Diagnostic Aphasia Examination 3rd Edition Severity Rating Scale),

Who the study is looking for

  • primary diagnosis of chronic stroke, ≥6 months post onset,
  • ≥18 years old,
  • community-dwelling (i.e., living in a residential setting in the community),
  • restrictions in social participation, indicated by Activity Card Sort (\<80% of pre-stroke activities)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Pittsburgh
Coordinator of this site? Confirm its status
PittsburghUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.