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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Illinois at Chicago

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of ESKD diagnosis and receiving hemodialysis for at least 3 months

Can read and speak English

Fatigue measured via visual analogue scale, score ≥4 over the last week

Able to stand and walk one block

Disqualifiers

Patient's nephrologist refuses for them to participate

Unstable angina

Unstable pulmonary disease or pulmonary symptoms that preclude participation

Lower-extremity amputation without prosthetic (BKA, AKA) -Orthopedic or neurologic condition that would preclude walking or tensing/releasing of muscles-

Trial design

Design model

Parallel

Treatments tested in this trial

  • Fight Fatigue

    Behavioral

    Combined progressive muscle relaxation and walking (increasing step count) 12-week intervention that consists of education/training followed by text messages.

  • Attention Control

    Other intervention

    End-stage kidney disease education

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Fight FatigueExperimental treatment 1 intervention
Group B: Attention ControlActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Feasibility of recruitment

Recruitment metrics (enrolled/invited)

Time frame
Baseline to week 12
2

Feasibility of retention

Retention in the study from baseline to week 12

Time frame
Baseline to week 12
3

Acceptability

Participant rating of acceptability (e.g., enjoyable, easy to understand) via Likert scale questions and open ended questions

Time frame
End of study (Week 12)
4

Adherence to the study protocol

Adherence to the intervention measured with adherence to step counts, number/duration of accesses on the study-specific website, and adherence to study procedures as evaluated with number of text messages read/sent messages read.

Time frame
Baseline to week 12

Secondary outcomes

Other outcomes

1

Fatigue

FACIT-Fatigue measure

Time frame
Baseline to week 12

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Illinois at Chicago

Lead sponsor

National Center for Complementary and Integrative Health (NCCIH)

Collaborator