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The Effect of Home Based Tel-Exercise on Dialysis Patients

NCT06313892 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-01-13

No results posted yet for this study

Summary

The objective of the trial is to assess key areas of uncertainty regarding the use of synchronous home-based tele exercise in future practice and research, including issues relating to feasibility, safety and potential for efficacy.

Conditions

Interventions

BEHAVIORAL

Home based Exercise

The participants in the study group will be given an online personalized exercise program at home in non dialysis days. Synchronous tele-exercise will be delivered using the free teleconference application (app) (Google Meets software). The groups of tele-exercises will be private and the professional will send the link for each training session and will control the access of the participants. Each session will be 40 to 45 min in duration for 3 days per week over 12 weeks, 36 sessions in total.

Sponsors & Collaborators

  • Pardis Specialized Wellness Institute

    lead OTHER

Principal Investigators

  • Mohammad Ali Tabibi, Dr · Pardis Specialized Wellness Institute

  • Bobby Cheema, Dr · School of Health Sciences, Western Sydney University, Campbelltow, NSW 2560, Australia

  • Tomas Wilkinson, Dr · Diabetes Research Centre, University of Leicester, Leicester, UK

  • Kenneth Wilund, Dr · School of Nutritional Sciences and Wellness, Arizona University

  • Fabio Manferedini, Dr · Dept of Neuroscience and Rehabilitation, University of Ferrara

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-15
Primary Completion
2024-06-12
Completion
2024-07-02

Countries

  • Iran

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06313892 on ClinicalTrials.gov