Skip to main content
Clinical Trials/NCT05876507
NCT05876507
Recruiting
Not Applicable

The Effects of Progressive Exercises on the Vital Signs and Fatigue in Patients With Renal Transplant

Baskent University1 site in 1 country52 target enrollmentFebruary 13, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Renal Transplant
Sponsor
Baskent University
Enrollment
52
Locations
1
Primary Endpoint
fatigue level
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

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

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.

Registry
clinicaltrials.gov
Start Date
February 13, 2023
End Date
June 15, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Seyda Uzun Yagız

Registered nurse

Baskent University

Eligibility Criteria

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

Outcomes

Primary Outcomes

fatigue level

Time Frame: Change from baseline at 4th week

Fatigue Severity Scale is a valid and 7-point Likert type scale. Possible scores range from 9-63. Higher scores indicate high level of fatigue. A score of 36 points or over indicates severe fatigue (Change= Lower score from the scale at the end of intervention compared to baseline).

Heart rate

Time Frame: Change from baseline at 4th week

Maintaining or normalizing heart rate within normal range (60 to 100 bpm)

Systolic and diastolic blood pressure

Time Frame: Change fron baseline at 4th week

Maintaining or normalizing systolic and blood pressure within normal range (systolic: 90-140 mmHg; diastolic 60-90 mmHg)

Body temperature

Time Frame: Change from baseline at 4th week

Maintaining or normalizing body temperature within normal range (36-37 C° in tympanic measurement)

Oxygen saturation

Time Frame: Change from baseline at 4th week

Maintaining or normalizing oxygen saturation within normal range (between 95%-100% by pulse oximetry)

Respiratory rate

Time Frame: Change from baseline at 4th week

Maintaining or normalizing respiratory rate within normal range (12-20 breath per minute)

Study Sites (1)

Loading locations...

Similar Trials