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Not yet recruitingNCT07758244Updated Aug 11, 2026

The Effects of Intradialytic Aerobic Exercise on Clinical Parameters, Coping With Illness, Perceived Benefits of Exercise and Barriers to Exercise in Haemodialysis Patients: A Randomised Controlled Trial

An interventional study of Exercise in Hemodialysis Patients, sponsored by Muş Alparslan University. Not yet recruiting. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-08-11.

Sponsored by Muş Alparslan University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

This randomized controlled trial aims to investigate the effects of an 8-week intradialytic aerobic exercise program on clinical parameters, disease adaptation, and perceived exercise benefits and barriers in patients undergoing maintenance hemodialysis. Eligible participants will be randomly assigned to either an intervention group receiving supervised aerobic exercise during hemodialysis sessions or a control group receiving routine hemodialysis care. Aerobic exercise will be performed three times per week during hemodialysis for eight weeks. Exercise intensity will be individually adjusted according to the participant's subjective fatigue level using the 20-point Borg Rating of Perceived Exertion (RPE) scale, targeting an intensity of 11-13 ("light to somewhat hard"). Outcomes will be assessed before and after the intervention using validated clinical measurements and patient-reported outcome measures.

02

Conditions studied

  • Hemodialysis Patients

Keywords

  • hemodialysis
  • aerobic exercise
  • adaptation to the disease
  • perceived exercise benefits
03

In context

Lead sponsor

Muş Alparslan University is the lead sponsor of 62 studies on the registry; 24 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Having received hemodialysis treatment for 4 hours a day, 3 days a week, for at least 3 months.

Exclusion criteria

Exclusion Criteria:

  • Having a history of myocardial infarction within the last 3 months
  • Having angina pectoris or uncontrolled arrhythmia and uncontrolled hypertension
  • Having communication or cognitive problems to the extent that one cannot complete the required tests
  • Being pregnant or undergoing infertility treatment
  • Having a psychiatric diagnosis
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Active comparator
    aerobic exercise

    Other: Exercise

  • No intervention
    control group

Interventions

  • OtherExercise

    The use of intradialytic aerobic exercise in hemodialysis patients.

06

What researchers measure

Primary outcomes

  1. Dialysis Patient-Perceived Exercise Benefits and Barriers Scale (DPEBBS)

    This is a 4-point Likert scale (1- Strongly Disagree, 4- Strongly Agree). The scale consists of 24 items and two open-ended questions. It comprises five sub-dimensions: "Daily Life (7 items)", "Exercise-related Undesirable Outcomes (7 items)", "Quality of Life (4 items)", "Exercise Effects (3 items)", and "Exercise Benefits (3 items)". The daily life and exercise-related undesirable outcomes sub-dimensions represent the obstacles to exercise, while the quality of life, exercise effects, and exercise benefits sub-dimensions represent the benefits of exercise. Items 3, 4, 6, 7, 10, 13, 16, 20, 22, and 23 comprise the benefits sub-dimension; items 1, 2, 5, 8, 9, 11, 12, 14, 15, 17-19, 21, and 24 comprise the obstacles sub-dimension. The items in the DPEBBS scale that represent barrier factors are reverse-coded. The scale is evaluated based on a total score (min=24, max=96). Higher scores indicate a greater perception of exercise benefits and fewer exercise barriers.

    Time frame: Two months

  2. The End-Stage Renal Disease Adherence Questionnaire (ESRD-AQ)

    The scale, designed to assess adherence to end-stage renal failure, consists of nine questions and four sub-dimensions encompassing adherence behaviors: "hemodialysis participation," "medication adherence," "fluid restriction adherence," and "diet adherence." The total score obtainable from the scale ranges from 0 to 1200. Higher scores indicate higher adherence to treatment.

    Time frame: Two months

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07758244
Lead sponsor
Muş Alparslan University
Responsible party
Sponsor
First posted
Aug 11, 2026
Start date
Aug 24, 2026 (estimated)
Primary completion
Aug 28, 2026 (estimated)
Completion
Oct 23, 2026 (estimated)
Last update
Aug 11, 2026

Study contacts

Cengiz TAŞKAYA
Contact
c.taskaya@alparslan.edu.tr
05364811882
Abdulsamed KAYA
Contact
a1@alparslan.edu.tr
05364400551
Cengiz TAŞKAYA
study director · Muş Alparslan University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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