Muscle Atrophy Clinical Trials

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Intrahospital Exercise Program in Hemodialysis Patients: Impact on Sarcopenia Markers, Sleep Quality, and Quality of Life.

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Sarcopenia (the loss of muscle mass, strength, and function) is highly prevalent in patients with Chronic Kidney Disease (CKD) undergoing hemodialysis, significantly increasing the risk of falls, frailty, and mortality. Despite its impact, there is a lack of evidence regarding the effectiveness of exercise programs specifically designed to address sarcopenia under the latest international diagnostic criteria (EWGSOP2) in older renal patients. The primary objective of this randomized controlled clinical trial is to evaluate the effects of a 12-week supervised intrahospital exercise program on muscle mass, strength, and physical performance in hemodialysis patients over 40 years of age. Additionally, the study aims to analyze how this intervention influences sleep quality-often disrupted in this population-and overall health-related quality of life. Participants will be randomly assigned to either an Intervention Group, which will perform personalized strength and aerobic exercises during the first 90 minutes of their dialysis sessions, or a Control Group, receiving standard care. Evaluations will be conducted at three points: baseline (pre-randomization), at 12 weeks (post-intervention). The investigators hypothesize that integrating physical exercise into the routine clinical care of hemodialysis patients will improve sarcopenia markers and sleep patterns, leading to greater functional independence and better clinical outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Healthy Volunteers: f
View:

• Subjects currently enrolled in a Chronic Hemodialysis Unit.

• Patients who have been on hemodialysis treatment for more than 3 months.

• Subjects aged 40 years or older.

• Hemoglobin levels greater than 10 mg/dl.

• Ability to perform physical fitness assessment tests or dynamometry.

• Willingness and ability to provide signed informed consent

Locations
Other Locations
Spain
Universidad de Salamanca
RECRUITING
Salamanca
Contact Information
Primary
María de la Luz Sánchez Tocino, PhD
mlsancheztocino@usal.es
+34 625067971
Time Frame
Start Date: 2026-01-02
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 58
Treatments
No_intervention: No Intervention : Control group
Experimental: Experimental: Intervention Group
Intradialytic exercise program (strength and aerobic) 3 times weekly for 3 months.
Related Therapeutic Areas
Sponsors
Collaborators: Gerencia Regional de Salud de Castilla y Leon, Instituto de Investigación Biomédica de Salamanca
Leads: University of Salamanca

This content was sourced from clinicaltrials.gov