Effect of Progressive Exercise on Renal Transplant Patients

NCT ID: NCT05876507

Last Updated: 2023-05-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

52 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-02-13

Study Completion Date

2023-06-15

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Renal Transplant Fatigue Vital Signs Progressive Relaxation Exercise Nursing

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

This is a single blind, randomized controlled study. The intervention group will receive an audio record explaining progressive relaxation exercise. Then participants will undergo training about the exercises. After training, the intervention group will perform the exercises at home by their own. The exercises will be performed everyday for 4 weeks about 25-30 minutes. Principal investigator will check the participants weekly about implementation of exercises.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Outcome Assessors
Double (Participant, Outcomes Assessor)

Study Groups

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exercise

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.

Group Type EXPERIMENTAL

Progressive relaxation exercise

Intervention Type BEHAVIORAL

Progressive relaxation exercises will take 25-30 minutes of patients daily.

Control

Participants will receive routine care.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Progressive relaxation exercise

Progressive relaxation exercises will take 25-30 minutes of patients daily.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Baskent University

OTHER

Sponsor Role lead

Responsible Party

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Seyda Uzun Yagız

Registered nurse

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Baskent University Hospital

Ankara, Çankaya, Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Şeyda Uzun Yağız, RN

Role: CONTACT

+905392791581

Sevcan Avcı Işık, PhD, RN

Role: CONTACT

+905433177016

Facility Contacts

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Şeyda Uzun Yağız, RN

Role: primary

+905392791581

Sevcan Avcı Işık, PhD, RN

Role: backup

+905433177016

Other Identifiers

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KA22/239

Identifier Type: -

Identifier Source: org_study_id

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