Progressive muscle relaxation to ease depression and fatigue during hemodialysis

Is this trial a fit for you?

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

What this trial studies

This randomized controlled trial delivers individualized progressive muscle relaxation (PMR) as a non‑pharmacological intervention for patients on maintenance hemodialysis and compares outcomes to usual care. Participants who can follow instructions and score at least 4 on the Beck Depression Inventory are randomized to regular PMR sessions while receiving hemodialysis or to a control group. Primary outcomes include changes in depressive symptoms and fatigue measured by standard scales, with assessments at baseline and after the intervention period. The study excludes patients with major psychiatric diagnoses, significant sensory or cognitive impairments, major musculoskeletal limitations, or regular prior practice of relaxation therapies and is conducted at Istanbul Aydın University.

Why it matters

Who can join: the full rules

Inclusion Criteria:

Scoring 4 or above on the First-Level Beck Depression Inventory

Patients who regularly receive hemodialysis treatment

Individuals who are cognitively capable of understanding the exercise instructions

Individuals who voluntarily agree to participate in the study and provide informed consent

Exclusion Criteria:

Individuals diagnosed with a psychiatric disorder (e.g., major depression, bipolar disorder, schizophrenia, etc.)

Individuals who are physically unable to perform relaxation exercises due to musculoskeletal disorders

Individuals who have previously participated regularly in relaxation therapy, yoga, meditation, or similar practices

Individuals who cannot follow instructions due to hearing, visual, or cognitive impairments

Individuals who are simultaneously participating in another psychosocial or physical intervention program

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Where it's running

• Istanbul Aydın Universty
  Istanbul, Istanbul, Turkey (Türkiye) Recruiting
• Arzu Kavala
  Istanbul, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: ARZU KAVALA, Assistant Prof
• Email: arzukavala@aydin.edu.tr
• Phone: +905445418208

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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.