Clinical trial Recruiting at 1 site Interventional Ages 18 to 80

Mindfulness during dialysis plus pre-dialysis strength training for sarcopenia in dialysis patients

Official title: A Study on the Clinical Efficacy and Safety Evaluation of Mindfulness Meditation During Dialysis Combined With Pre-Dialysis Progressive Resistance Training for Hemodialysis Patients With Sarcopenia

Run by Ningbo Medical Center Lihuili Hospital · NCT07724587 · Data updated 2026-11-12

This study tests whether adding mindfulness meditation during dialysis to pre-dialysis resistance training helps improve muscle mass and safety in adults undergoing maintenance hemodialysis with sarcopenia.

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment76 (estimated)
SponsorNingbo Medical Center Lihuili Hospital
Government
Locations1 site (Ningbo)
StatusRecruiting
StartedSeptember 1, 2025
Main results expectedDecember 1, 2026
Study endsDecember 1, 2026
Registry record updatedJuly 24, 2026
Trial IDNCT07724587 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults on regular hemodialysis (3 times/week) for at least 3 months with sarcopenia who can participate in supervised exercise.

Probably not a fit

Patients unable to participate in supervised exercise or mindfulness training, or those with recent major cardiovascular events or cognitive impairment, may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In this randomized trial, 76 maintenance hemodialysis patients with sarcopenia are assigned to three groups: a control group receiving standard care, a sports group doing pre-dialysis resistance training, and an intervention group that adds mindfulness meditation during dialysis. Outcomes including muscle mass via ultrasound, sleep quality, anxiety, and depression are assessed at baseline and 12 weeks, with blinded assessors to reduce bias. The program follows a four-part protocol: assessment and education, one-repetition maximum testing, pre-dialysis resistance training, and mindfulness training during dialysis. The study design aims to determine if the combined intervention is safe and more effective than exercise or standard care alone.

Why it matters

Potential benefit: If successful, patients may experience better muscle mass and well-being with a feasible, non-pharmacologic approach.

How similar studies have gone: Previous evidence supports exercise-based approaches for sarcopenia in dialysis patients; adding mindfulness is exploratory and less established.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Meet the updated Asian diagnostic criteria for sarcopenia
* Stable vital signs and general physical condition
* Willing and able to cooperate with supervised exercise training
* Regular hemodialysis 3 times per week for at least 3 months

Exclusion Criteria:

* Acute cardiovascular or cerebrovascular events within the previous 3 months
* Cognitive dysfunction affecting study cooperation and exercise completion
* Severe osteoarticular or limb movement disorders preventing standardized exercise training
* Active systemic infection

Where it's running

  • Yongyao Wu
    Ningbo, China
    Recruiting

Study contacts

  • Principal investigator: yongyao wu — Department of Nephrology, Ningbo Medical Center Li Huili Hospital
  • Study coordinator: yongyao wu
  • Email: wuyongyao.12345@163.com
  • Phone: 8615967857855

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.