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Effect of Progressive Exercise on Renal Transplant Patients

B

Baskent University

Status

Enrolling

Conditions

Vital Signs
Progressive Relaxation Exercise
Nursing
Fatigue
Renal Transplant

Treatments

Behavioral: Progressive relaxation exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT05876507
KA22/239

Details and patient eligibility

About

The goal of this interventional study is to determine the effect of progressive relaxation exercises on the vital signs and fatigue levels of patients with renal transplantation.

Full description

Renal transplant patients experience intense level of fatigue as well as vital sign problems due to treatment protocol. This research is designed to determine the effect of progressive relaxation exercises on vital signs and fatigue level of patients with renal transplantation.

In this study, the participants will be randomized in a single blind manner (participant) to either intervention (4 week exercise program) or control (routine care) groups.

Enrollment

52 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients underwent renal transplant within one year from the beginning of the study
  • Patients having no communication problems
  • Patients having a smart phone either own or o family member

Exclusion criteria

  • Patients having musculoskeletal, cardiopulmonary, or psychiatric disorders

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

52 participants in 2 patient groups

exercise
Experimental group
Description:
Participants will receive a training about progressive relaxation exercises on the first day, then given an audio-record containing instructions about exercises. They will perform exercises at home for 4 week and revisited by the principal investigator at the 2nd and 4th week.
Treatment:
Behavioral: Progressive relaxation exercise
Control
No Intervention group
Description:
Participants will receive routine care.

Trial contacts and locations

1

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Central trial contact

Şeyda Uzun Yağız, RN; Sevcan Avcı Işık, PhD, RN

Data sourced from clinicaltrials.gov

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