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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04935645
Other study ID # Mardin Artuklu University
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2019
Est. completion date December 30, 2020

Study information

Verified date June 2021
Source Mardin Artuklu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients undergoing colonoscopy were divided into progressive relaxation exercises and control groups. Pretest and posttest abdominal pain and distention scores of the patients were determined after colonoscopy.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date December 30, 2020
Est. primary completion date December 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients undergoing colonoscopy - Those who do not have communication problems, - After the colonoscopy procedure, the abdominal pain score is evaluated by VAS and is 4 or higher, - Evaluation of the distension score of 4 and above with VAS after the colonoscopy procedure, - Be 18 years old or older. Exclusion Criteria: - Being a hospitalized patient undergoing colonoscopy, - Be younger than 18 years old - To have used complementary and alternative methods during the research, - Any physical problem that may prevent you from doing the exercises, - Having a cognitive illness - Refusing to participate in the research, - Failing to complete surveys.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Progressive Muscle Relaxation
PMR is a technique that provides relaxation in the whole body by voluntary and regular relaxation of large muscle groups in the human body, which is included in mind-body applications.

Locations

Country Name City State
Turkey Mardin State Hospital Mardin

Sponsors (1)

Lead Sponsor Collaborator
Mardin Artuklu University

Country where clinical trial is conducted

Turkey, 

References & Publications (5)

Lahmann C, Röhricht F, Sauer N, Noll-Hussong M, Ronel J, Henrich G, von Arnim A, Loew T. Functional relaxation as complementary therapy in irritable bowel syndrome: a randomized, controlled clinical trial. J Altern Complement Med. 2010 Jan;16(1):47-52. do — View Citation

Levy I, Gralnek IM. Complications of diagnostic colonoscopy, upper endoscopy, and enteroscopy. Best Pract Res Clin Gastroenterol. 2016 Oct;30(5):705-718. doi: 10.1016/j.bpg.2016.09.005. Epub 2016 Sep 14. Review. — View Citation

Pan CX, Morrison RS, Ness J, Fugh-Berman A, Leipzig RM. Complementary and alternative medicine in the management of pain, dyspnea, and nausea and vomiting near the end of life. A systematic review. J Pain Symptom Manage. 2000 Nov;20(5):374-87. — View Citation

Park DI, Kim HJ, Park JH, Cho YK, Sohn CI, Jeon WK, Kim BI, Ryu SH, Sung IK. Factors affecting abdominal pain during colonoscopy. Eur J Gastroenterol Hepatol. 2007 Aug;19(8):695-9. — View Citation

Steffenssen MW, Al-Najami I, Baatrup G. Patient-reported minor adverse events after colonoscopy: a systematic review. Acta Oncol. 2019;58(sup1):S22-S28. doi: 10.1080/0284186X.2019.1574979. Epub 2019 Feb 20. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Individual Introductory Information Form This form, which was created by the researcher with the support of the relevant literature, consists of 11 questions questioning the patients' education level, age,gender, employment status, marital status,income level, the coping methods they use when there is distension in their daily lives, the coping methods they use when there is pain in their daily lives, the status of having a colonoscopy before, the history of abdominal pain and distension of those who have a colonoscopy experience. 15 minutes
Secondary Visual Analogue Scale (VAS) The patient was asked to make a mark on a 10 cm horizontal line on the Visual analog scale showing his current state. In this study, for pain and distension; Markings were made on a 10 cm horizontal line, one end of which indicates that the patient's pain is very good (0 = no pain) and the other end is that the patient's pain is very bad (10 = most severe). The distance from the point where there was no pain and distension (0) to the point marked by the patient was measured. The value found shows the severity of pain and distention of the patient. 10 minutes
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