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The Effect of Progressive Muscle Relaxation on Abdominal Pain and Distension in Colonoscopy Patients.

The Effect of Progressive Muscle Relaxation on Abdominal Pain and Distension in Colonoscopy Patients.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04935645
Enrollment
90
Registered
2021-06-23
Start date
2019-07-01
Completion date
2020-12-30
Last updated
2021-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Pain

Keywords

Colonoscopy, Abdominal Pain, Nursing, relaxation, exercise

Brief 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.

Interventions

BEHAVIORALProgressive 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.

Sponsors

Mardin Artuklu University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Individual Introductory Information Form15 minutesThis 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.

Secondary

MeasureTime frameDescription
Visual Analogue Scale (VAS)10 minutesThe 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026