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NCT05568524Completed

Resistance Training With Blood Flow Restriction in Hemophilia

The Acute and Chronic Impact of Blood Flow Restriction Resistance Training on Physical and Neuromuscular Function, Pain, and Quality of Life in Patients With Moderate/Severe Hemophilia

Source: ClinicalTrials.gov · Last updated 3 Feb 2026

Brief summary (registry, in English)

The main objectives of this study are to evaluate safety and chronic effects of a low-load resistance exercise intervention (elbow flexions and extensions, and knee extensions) with blood flow restriction in people with hemophilia on quality of life, pain, and on physical and neuromuscular function.

Status (registry)
Completed
Study type
Interventional
Enrollment
20 (actual)
First submitted
29 Sept 2022
Start date
15 Jan 2024
Primary completion date
30 Jan 2026
Lead sponsor
University of Valencia
Diseases
Haemophilia
NCT number
NCT05568524

What you commit to

  • Study type: Interventional
  • Participants enrolled: 20
  • From 15 Jan 2024 to the primary completion date, 30 Jan 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.

Prior treatment

  • surgical procedures performed 6 weeks prior to or during the exercise program; - participation in any other form of exercise, not previously done, during the study;
  • changes in medication during the study;
  • need for major surgery;

Other illness

  • a major bleeding episode that posed a risk or prevented exercise;

Other

  • the inability to attend exercise sessions at least twice a week for 8 consecutive weeks;
  • non adherence to instruction on proper exercise technique;
  • another hemostatic defect;
  • withdrawal of informed consent.

Who the study is looking for

  • diagnosis of hemophilia A or B and undergoing prophylaxis;
  • willingness to exercise twice a week during the training program and to complete the pre- and post-program evaluations;
  • approval by their hematologist to participate in the exercise program;
  • age between 18 and 60 years;
  • informed consent signed.

Age in the registry: 18 years to 60 years · Sex: Male · 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
Facultat de Fisioteràpia
Coordinator of this site? Confirm its status
ValenciaSpainUnknown status

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