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NCT07579871Recruiting

Sleep and Stroke Rehabilitation Study

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

The study aims to map sleep disorders and their impact on the ability to engage in an active daily life among people who have had a stroke, with particular focus on how sleep apnea can be identified. The study has the following objectives: 1. To examine the occurrence of sleep apnea, insomnia, excessive daytime sleepiness, and restless legs syndrome/periodic limb movements in patients with ischemic stroke three months after onset. 2. To investigate associations between these sleep disorders and physical and mental health, fatigue, quality of life, cognitive and physical function, and daily physical behavior including physical activity levels. 3. To identify which clinical factors and patient reported data, including patient reported data from commercial wearable health technology, predict a diagnosis of sleep apnea. 4. To examine how sleep disorders affect changes in physical and mental health, fatigue, quality of life, cognitive and physical function, and daily physical behavior including physical activity levels one year after stroke.

Status (registry)
Recruiting
Study type
Observational
Enrollment
226 (estimated)
First submitted
27 Feb 2026
Start date
18 Mar 2026
Primary completion date
30 Oct 2028
Lead sponsor
Malin Eleonora av Kák Gustafsson, MD, PhD
Diseases
Stroke
NCT number
NCT07579871

What you commit to

  • Study type: Observational
  • Planned participants: 226
  • From 18 Mar 2026 to the primary completion date, 30 Oct 2028
  • 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

  • Unable to carry HSAT equipment (e.g., gel nails; the patient is wearing other medical devices; motor or cognitive impairment without the possibility of assistance from healthcare staff or relatives).

Other

  • Short expected survival.
  • Reduced understanding of the project due to insufficient Swedish, which cannot be bridged with an interpreter.

Who the study is looking for

  • Ischemic stroke.
  • First time stroke.

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
Skånes Universitetssjukhus, SUS
Coordinator of this site? Confirm its status
LundSwedenRecruiting

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