Skip to main content
Clinical Trials/NCT06584019
NCT06584019CompletedNot Applicable

The Effect of Range of Motion (ROM) Exercises Applied to Oncology Patients in the 6-12 Years Group on the Comfort Level and Vital Signs

Istanbul Medipol University Hospital1 site in 1 country30 target enrollmentStarted: May 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Pulse

Study Overview

Brief Summary

This experimental study aims to examine the effects of ROM (Range of Motion) exercises on comfort level and vital signs in children diagnosed with cancer.

Detailed Description

The sample of the study consisted of a total of 60 oncology patient children, 30 in the experimental group and 30 in the control group, between the ages of 6-12, who were hospitalized in the Pediatric Bone Marrow Transplant Unit and Pediatric Hematology Oncology Service of a state hospital. The data of the study were collected with the "Data Collection Form", "Life Findings Table" and "Comfort Scale in Children". Range of motion exercise applications continued once a day for 5 days a week for approximately 20 minutes. Fever, pulse, respiration, blood pressure, pain and comfort levels of the children were measured before and after the exercise. In the study, it was investigated whether Range of motion exercises have an effect on vital signs and comfort levels of children with cancer.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Investigator)

Eligibility Criteria

Ages
6 Years to 12 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Individuals between 6 and 12 years of age.
  • •Patients diagnosed with oncology.
  • •Patients who agreed to participate in the study and whose consent was obtained from their parents.
  • •Patients who can communicate and are conscious.

Exclusion Criteria

  • •Patients with fractures or orthopedic conditions that may limit exercise.
  • •Patients with serious cardiac problems that may prevent exercise.

Arms & Interventions

Range Of Motion applied group

Experimental

Children with cancer were given Range Of Motion exercises once a day for 5 days for approximately 20 minutes.

Intervention: Range Of Motion applied group (Other)

Control group

No Intervention

Children with cancer in this group received no intervention.

Outcomes

Primary Outcomes

Pulse

Time Frame: For 5 days/ 2 times a day/ before and after a 20 minute range of motion.

For 5 days, children's pulse was taken 2 times before and after 20 minutes of Range Of Motion.

Respiration

Time Frame: For 5 days/ 2 times a day/ before and after a 20 minute range of motion.

For 5 days, children's Respiration was taken 2 times before and after 20 minutes of Range Of Motion.

Body temperature

Time Frame: For 5 days/ 2 times a day/ before and after a 20 minute range of motion.

For 5 days, children's body temperature was taken 2 times before and after 20 minutes of Range Of Motion.

Blood pressure

Time Frame: For 5 days/ 2 times a day/ before and after a 20 minute range of motion.

For 5 days, children's systolic blood pressure and diastolic blood pressure was taken 2 times before and after 20 minutes of Range Of Motion.

Comfort

Time Frame: For 5 days/ 2 times a day/ before and after a 20 minute range of motion.

For 5 days, children's comfort level was taken 2 times before and after 20 minutes of Range Of Motion. Pediatric Comfort Assessment Scale was used for measurement. It evaluates 5 parameters: sounds, motor movements, performance, facial expressions and other. Each item is evaluated on a 5-point Likert scale from 0 to 4 (0/Not Available, 1/No, 2/Somewhat, 3/Moderate, 4/Strong) from bad to good. Higher scores indicate a higher level of comfort.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Istanbul Medipol University Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

aysel kokcudogan

Ph.D., Asst. Prof.

Istanbul Medipol University Hospital

Study Sites (1)

Loading locations...

Similar Trials