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Feasibility BFRT Geriatric Stroke Patients - Trial NCT06398041

Access comprehensive clinical trial information for NCT06398041 through Pure Global AI's free database. This phase not specified trial is sponsored by Universitaire Ziekenhuizen KU Leuven and is currently Not yet recruiting. The study focuses on Stroke. Target enrollment is 16 participants.

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NCT06398041
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Trial Details
ClinicalTrials.gov โ€ข NCT06398041
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Feasibility BFRT Geriatric Stroke Patients
Feasibility of Blood Flow Restriction Training in Stroke Patients on a Geriatric Ward

Study Focus

Stroke

Blood flow restriction training

Interventional

other

Sponsor & Location

Universitaire Ziekenhuizen KU Leuven

Pellenberg, Belgium

Timeline & Enrollment

N/A

May 01, 2024

Oct 01, 2025

16 participants

Primary Outcome

Proportion of eligible individuals and their willingness to undergo BFRT,Prevalence and types of Adverse events,Rate of attended sessions over the total number of sessions planned,Visual Analog Scale for feelings of perceived pain, effort, safety and comfort,Time investment,Feasibility assessed by the physiotherapist,Feasibility assessed by the patients

Summary

The focus of this interventional study is to assess the feasibility of blood flow restriction
 training (BFRT) in a geriatric stroke population. Patients will undergo a 4-week program of
 BFRT additionally to our standard physiotherapy, conducted twice weekly by experienced
 physiotherapists.
 
 The main goal of the study is to assess its feasibility concerning the safety and tolerance
 of BFRT from a patients and therapists scope. Furthermore, the investigators want to
 establish the proportion of eligible individuals & their willingness to undergo BFRT, as well
 as the time investment.
 
 The feasibility of an effectiveness study and potential sample size will be evaluated aside.

ICD-10 Classifications

Stroke, not specified as haemorrhage or infarction
Sequelae of stroke, not specified as haemorrhage or infarction
Cerebral infarction
Family history of stroke
Cerebral infarction, unspecified

Data Source

ClinicalTrials.gov

NCT06398041

Non-Device Trial