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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06333535
Other study ID # 2022/568
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2023
Est. completion date February 25, 2024

Study information

Verified date March 2024
Source TC Erciyes University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study was to determine the effect of foot and abdominal massage applied to after colonoscopy on abdominal distention, pain and patient satisfaction.This was a randomized controlled experimental study conducted at the Colonoscopy unit in Medica Faculty Hospital . Participants assigned to the intervention group-1 received foot massages after colonoscopy, participants assigned to the intervention group-2 received abdominal massages after colonoscopy and participants assigned to the intervention group-3 received foot and abdominal massages after colonoscopy. Participants assigned to the control group received only "routine care" after colonoscopy. The abdominal pain, distension and satisfaction levels of the patients evaluated using the Numerical Rating Scale


Description:

The aim of this study was to determine the effect of foot and abdominal massage applied to after colonoscopy on abdominal distention, pain and patient satisfaction.This was a randomized controlled experimental study conducted at the Colonoscopy unit in Medica Faculty Hospital . Participants meeting inclusion criteria were assigned to intervention and control groups using a random. Participants assigned to the intervention group-1 received foot massages after colonoscopy, participants assigned to the intervention group-2 received abdominal massages after colonoscopy and participants assigned to the intervention group-3 received foot and abdominal massages after colonoscopy. Participants assigned to the control group received only "routine care" after colonoscopy. The abdominal pain, distension and satisfaction levels of the patients evaluated using the Numerical Rating Scale


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date February 25, 2024
Est. primary completion date January 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Being of 18 years of age and above - Applying for colonoscopy for diagnosis and treatment, - Being conscious and oriented to place, person and time, - Having pain after the procedure, - No communication barriers, - Able to communicate in Turkish, - Individuals who gave written consent to participate in the research were included in the study. Exclusion Criteria: - Having any psychiatric disease, - Those who have previously had bowel resection or another bowel surgery, - Those with colostomy and ileostomy, - Those with percutaneous endoscopic gastrostomy, - Those with Inflammatory Bowel Disease, - Having a history of malignant intestinal obstruction in their health history, - Diagnosed with colon cancer, - Those with umbilical/abdominal hernia, - Having an open wound in the abdominal and/or foot area, - Those with active lower gastrointestinal system bleeding, - Those with celiac disease, - Patients with FMF disease were excluded from the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
foot massage
foot massage
abdominal massage
abdominal massage
foot and abdominal massage
foot and abdominal massage

Locations

Country Name City State
Turkey Erciyes University Kayseri

Sponsors (1)

Lead Sponsor Collaborator
TC Erciyes University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary abdominal pain Abdominal pain evaluated with the Numerical Rating Scale Scale Zero = minimum value Ten = maximum value The end of the colonoscopy (0. Min), the end of intervention 30.min., 2. hour and 4. hour ]
Primary Abdominal distension Abdominal distension evaluated with the Numerical Rating Scale Scale Zero = minimum value Ten = maximum value The end of the colonoscopy (0. Min), the end of intervention 30.min., 2. hour and 4. hour
Primary Patient Satisfaction Satisfaction evaluated with the Numerical Rating Scale Scale Zero = minimum value Ten = maximum value The end of intervention 4. hour
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