Healthy Clinical Trial
Official title:
The Effect of Post Colonoscopy Abdominal Massage on Abdominal Pain, Distension, Discomfort and Patient Satisfaction: A Randomized Controlled Study Protocol
Verified date | July 2021 |
Source | Prof. Dr. Cemil Tascioglu Education and Research Hospital Organization |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Background: Abdominal pain, distension, and discomfort are the most frequently seen side effects after colonoscopy. These side effects can cause physical and mental results and increased workloads and care costs. Additionally, the satisfaction of the patients with the colonoscopy process may affect their willingness to undergo repeated colonoscopies in the future which may be required for the surveillance of colon malignity. Currently, there are no studies evaluating the effects of abdominal massage on post colonoscopy these abdominal symptoms. The aim of this study was to evaluate the effect of post colonoscopy abdominal massage on abdominal pain, distension, discomfort, and patient satisfaction. Methods: This study was designed as a prospective randomized controlled study. Participants meeting inclusion criteria will be assigned to intervention and control groups using a random number generator. Participants assigned to the intervention group will receive abdominal massages twice a day after colonoscopy, and participants assigned to the control group will receive only "routine care". The abdominal pain, distension, discomfort, and satisfaction levels of the patients will be evaluated using the Visual Analogue Scale. Conclusions: New approaches are needed to improve the physiological and psychological health levels of patients after colonoscopy and help them return to their daily life activities and social lives faster. The trial will provide valuable evidence to inform clinical application and help evaluate the effects of the use of the relevant intervention.
Status | Active, not recruiting |
Enrollment | 180 |
Est. completion date | October 31, 2021 |
Est. primary completion date | May 31, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - being of 18 years of age and above - owning a cell phone - having a body mass index below 30 - being conscious and having location - people, and time orientation - having no communication barriers - being able to communicate in Turkish - giving written informed consent to participate in the study Exclusion Criteria: - were receiving sedation - having previously received intestine resection or other intestinal surgery - having an uncontrolled psychopathological illness - receiving colonoscopy for treatment - having active lower gastrointestinal system bleeding |
Country | Name | City | State |
---|---|---|---|
Turkey | Prof. Dr. Cemil Tascioglu City Hospital | Istanbul |
Lead Sponsor | Collaborator |
---|---|
Prof. Dr. Cemil Tascioglu Education and Research Hospital Organization |
Turkey,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Comfort | Abdominal comfort will be evaluated with the Visual Analog Scale Zero = minimum value Ten = maximum value | The end of the second day. | |
Other | High Satisfaction | Patient satisfaction will be evaluated with the Visual Analog Scale Zero = minimum value Ten = maximum value | The end of the second day. | |
Primary | Abdominal pain | Abdominal pain will be evaluated with the Visual Analog Scale Zero = minimum value Ten = maximum value | The end of the second day. | |
Secondary | Abdominal distension | Abdominal distension will be evaluated with the Visual Analog Scale Zero = minimum value Ten = maximum value | The end of the second day. |
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