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NCT06660160Active, not recruiting

Group Exercise Program Supported By Audiovisual Media During Hemodialysis

Evaluating The Feasibility And Safety Of A Group Exercise Program Supported By Audiovisual Media During Hemodialysis (GrExID)

Source: ClinicalTrials.gov · Last updated 2 Nov 2026

Brief summary (registry, in English)

People with chronic kidney disease (CKD) undergoing hemodialysis (HD) experience muscular complications, such as sarcopenia, which worsen their functional capacity and increase mortality. Exercise programs during HD are an effective strategy to combat sedentary behavior, and implementing them through innovative technologies could facilitate their adoption in clinics, benefiting more patients. Therefore, the study's objectives are to assess the feasibility and safety of a group exercise program supported by audiovisual media conducted during HD sessions. Additionally, it will analyze factors influencing adherence, identify potential causes for interruptions or failure to perform the prescribed exercise, and evaluate the risk and prevalence of sarcopenia, its association with low muscle strength, poor muscle quality, and physical inactivity.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
45 (estimated)
First submitted
18 Oct 2024
Start date
28 Oct 2024
Primary completion date
29 May 2025
Lead sponsor
Cardenal Herrera University
NCT number
NCT06660160

What you commit to

  • Study type: Interventional
  • Planned participants: 45
  • From 28 Oct 2024 to the primary completion date, 29 May 2025
  • 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

  • Undergoing high doses of corticosteroids (\>30 mg/day);

Other illness

  • Neurological, musculoskeletal, or osteoarticular disorders;

Other

  • Lower limb amputations;
  • Severe and unstable comorbidities;
  • Inability to understand the measurement methods used.

Who the study is looking for

  • Over 18 years old of both sexes;
  • Undergoing HD for at least three months in three sessions per week, four hours, totaling 12 hours per week.

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
B. Braun Avitum - Centro de Atención Renal
Coordinator of this site? Confirm its status
MassamagrellSpainUnknown status

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