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NCT07444151Recruiting

Post-Stroke Fatigue Perception Study (ReFast)

Exploration of Subjective Post-Stroke Fatigue: A Mixed-Methods Questionnaire Study (ReFast - Recovery and Fatigue Study)

Source: ClinicalTrials.gov · Last updated 2 Mar 2026

Brief summary (registry, in English)

The goal of this observational study is to better understand fatigue after stroke. Many people feel ongoing tiredness months or years after a stroke. This fatigue may affect daily activities, work, and social life. It does not always improve with rest. This study aims to answer these questions: How do participants describe their fatigue? How strong and how often does it occur? How does it affect daily life and quality of life? What strategies do participants use to manage it? About 20 to 30 adults living in French-speaking Switzerland who have had a stroke will take part. Participants will: Complete one anonymous questionnaire online or on paper. Answer questions about their fatigue and daily life. Share their experience in their own words. The questionnaire takes about 15 to 20 minutes. There are no medical tests, treatments, or follow-up visits. Participation is voluntary. Participants may stop at any time. No names or identifying information are collected. The results may help health professionals better understand post-stroke fatigue and improve rehabilitation care.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
16 Feb 2026
Start date
27 Jan 2026
Primary completion date
31 Dec 2026
Lead sponsor
School of Health Sciences Geneva
Diseases
Stroke
NCT number
NCT07444151

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 27 Jan 2026 to the primary completion date, 31 Dec 2026
  • 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

  • Transient ischemic attack (TIA) without confirmed stroke
  • History of two or more strokes
  • Fatigue primarily caused by another chronic medical condition (e.g., cancer, primary depression, multiple sclerosis)
  • Severe cognitive or communication impairment preventing independent completion of the questionnaire

Other

  • Currently institutionalized (e.g., nursing home, long-term hospital care, rehabilitation center)
  • Unable to understand written French

Who the study is looking for

  • Age 18 years or older
  • Living in French-speaking Switzerland
  • Confirmed history of ischemic or hemorrhagic stroke
  • Self-reported fatigue attributed to stroke
  • Living in the community (not institutionalized)
  • Able to read and understand written French
  • Able to provide informed consent

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
Haute école de santé de Genève (HEdS - HES-SO)
Coordinator of this site? Confirm its status
CarougeSwitzerlandRecruiting

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