Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07014111

Fight Fatigue: A Progressive Muscle Relaxation and Walking Intervention to Reduce Fatigue in Adults With ESKD

Led by University of Illinois at Chicago · Updated on 2025-09-26

40

Participants Needed

1

Research Sites

91 weeks

Total Duration

On this page

Sponsors

U

University of Illinois at Chicago

Lead Sponsor

N

National Center for Complementary and Integrative Health (NCCIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Fight Fatigue is evaluating the feasibility and acceptability of a combined progressive muscle relaxation and walking intervention to reduce fatigue for adults with end-stage kidney disease receiving in-center hemodialysis.

CONDITIONS

Official Title

Fight Fatigue: A Progressive Muscle Relaxation and Walking Intervention to Reduce Fatigue in Adults With ESKD

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of end-stage kidney disease and receiving hemodialysis for at least 3 months
  • Ability to read and speak English
  • Fatigue score of 4 or higher on visual analogue scale over the last week
  • Able to stand and walk one block
  • Has a cell phone that can receive text messages
Not Eligible

You will not qualify if you...

  • Nephrologist refuses permission to participate
  • Unstable angina
  • Unstable pulmonary disease or symptoms preventing participation
  • Lower-extremity amputation without prosthetic (below or above knee)
  • Orthopedic or neurologic condition preventing walking or muscle relaxation exercises
  • Cognitive impairment preventing participation as judged by research team
  • Participation in the formative phase of the Fight Fatigue development

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UI Health/University of Illinois Chicago

Chicago, Illinois, United States, 60612

Actively Recruiting

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Research Team

M

Mary Hannan, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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