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NCT06588647Recruiting

Improving Participation After Stroke Self-Management-Rehabilitation

Efficacy of the Improving Participation After Stroke Self-Management-Rehabilitation (IPASS-R) Program in Sub-acute Stroke

Source: ClinicalTrials.gov · Last updated 28 Apr 2026

Brief summary (registry, in English)

The overall goal of this proposed study is to evaluate the efficacy of a small-group, stroke-specific, self-management program delivered via telehealth to improve self-efficacy, activity performance, and quality of life in individuals with sub-acute stroke.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
6 Sept 2024
Start date
16 Dec 2024
Primary completion date
15 Dec 2029
Lead sponsor
University of Missouri-Columbia
Diseases
Stroke
NCT number
NCT06588647

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 16 Dec 2024 to the primary completion date, 15 Dec 2029
  • 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.

Prior treatment

  • additional neurological diagnoses (e.g., brain malignancy, previous severe stroke)

Other illness

  • dementia symptoms as indicated by a score of \<23 on the Montreal Cognitive Assessment
  • (4) moderate or severe aphasia as indicated by a National Institutes of Health Stroke Scale aphasia score of ≥ 2
  • any other condition not otherwise specified that the PI determines would render participation in this study as unsafe for the participant

Other

  • severe depressive symptoms as indicated by a score ≥21 on the Patient Health Questionnaire
  • inability to provide informed consent

Who the study is looking for

  • less than 6 months post-stroke
  • age 45-85 years
  • completed inpatient rehabilitation services (if recommended)
  • living in the community with or without caregiver support (i.e., not living in a skilled nursing facility)
  • ability to read, write, and speak English
  • diagnosis of mild or moderate stroke (National Institutes of Health stroke score \<16)
  • able to use videoconferencing independently or with caregiver support

Age in the registry: 45 years to 85 years · 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 Missouri
Coordinator of this site? Confirm its status
ColumbiaUnited StatesRecruiting

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