Abdominal Pain Clinical Trial
Official title:
The Effect of Foot and Abdominal Massage Applied to After Colonoscopy on Abdominal Distention, Pain and Patient Satisfaction
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 |
Verified date | March 2024 |
Source | TC Erciyes University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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
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. |
Country | Name | City | State |
---|---|---|---|
Turkey | Erciyes University | Kayseri |
Lead Sponsor | Collaborator |
---|---|
TC Erciyes University |
Turkey,
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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