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OpenTrials
Completed

NCT Number: NCT04935645

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

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.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mardin State Hospital

Mardin, 47000, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Progressive Muscle Relaxation

Behavioral

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.

Primary outcomes

  1. Individual Introductory Information Form

    Time frame: 15 minutes

    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.

Secondary outcomes

  1. Visual Analogue Scale (VAS)

    Time frame: 10 minutes

    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.

Sponsors and collaborators

Lead sponsor

Mardin Artuklu University

Other

Registry information

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Jun 23, 2021
Registry last updated
Jun 23, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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