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NCT Number: NCT04466319

The Effect of Rocking Chair Movement on the Start of Bowel Functions in Patients With Gastrointestinal System Surgery

The Effect of Rocking Chair Movement on the Start of Bowel Functions in Patients With Gastrointestinal System Surgery

The research will be carried out as a randomized controlled experimental study in patients with open gastrointestinal tract surgery in order to evaluate the effect of rocking chair movement to be given in addition to standard care in the initiation of postoperative bowel functions (post-operative first time gas, first time defecation).Ethics committee and institution permissions and written consents of individuals were obtained prior to the study.The universe of the study was composed of patients with open gastrointestinal surgery lying in the general surgery service of a hospital in Eskisehir. With the error margin of 0.05, 90% test power, 30 people in intervention and control groups, 60 patients in total will be included in the research.Appointment of patients to intervention and control groups was done by stratification and block randomization method according to gastric and intestinal surgery.The draw method was used to assign stratified patients to blind technique intervention and control groups in order to avoid side-holding, and an equal number (blocking) patients were assigned to each group. The individuals in the intervention group in the rocking chair three times a day, 20 minutes, a total of 60 minutes after the first day after surgery. The individuals in the control group will sit in a standard chair in the same time as the intervention group in the non-rocking chair. The data will be collected using the "Descriptive characteristics determination form", "Intervention Group Intestinal Functions Evaluation Form" and "Control Group Intestinal Functions Evaluation Form".

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Dean of the Faculty of Medicine Ground Floor Meşelik Campus

Eskişehir, Odunpazarı, 26040, Turkey (Türkiye)

About this study

Inclusion criteria

  • Accepting to participate in the research
  • Being 18 or over
  • Having gastrointestinal surgery
  • No communication problems
  • No symptoms or disease (dizziness, Vertigo, Meniere.) That rocking chair movement will adversely affect the patient
  • With or without a stoma in the postoperative period;
  • Patients with ASA (American Society of Anesthesiology) classification I or II

Exclusion criteria

  • Not agreeing to participate in the research
  • Being 18 or under
  • Being a communication problem
  • The symptoms or disease (dizziness, Vertigo, Meniere.) That the rocking chair movement will adversely affect the patient.
  • Having a history of ileus after surgery
  • Any complication after surgery
  • With inflammatory and irritable bowel disease
  • Using drugs that will affect intestinal motility before or after surgery.
  • Surgical intervention is laparoscopic
  • ASA classification is III, IV or V

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Agree to participate in the research
  • Being 18 or over
  • Having gastrointestinal surgery
  • No communication problems
  • No symptoms or disease (dizziness, Vertigo, Meniere.) That rocking chair movement will adversely affect the patient With or without a stoma in the postoperative period;
  • Patients with American Society of Anesthesiology (ASA) classification I or II

Exclusion criteria

  • Not agreeing to participate in the research
  • being 18 or under
  • Being a communication problem
  • The symptoms or disease (dizziness, Vertigo, Meniere.) That the rocking chair movement will adversely affect the patient.
  • Having a history of ileus after surgery
  • Any complication after surgery
  • With inflammatory and irritable bowel disease
  • Using drugs that will affect intestinal motility before or after surgery.
  • Surgical intervention is laparoscopic
  • ASA classification is III, IV or V

Treatment and study plan

Rocking Chair

Other

Patients in the experimental group were sat rocking chair three times a day in a rocking wooden chair in addition to their postoperative routine care by their nurses. After providing the rocking chair to the patients' room, the researcher gave the data collection form to be filled by the patient himself. It was the researcher's supervision that the patient sat in the rocking chair for the first time. The rocking chair movement continued to intervene until the patient released gas. After emitting gas, he continued to swing in the rocking chair until he made his first stools. The patient was visited every day until he was discharged. No special clothing or materials were required for the patients to sit in the rocking chair.

Primary outcomes

  1. time to report of first flatus

    Time frame: Defined as the first time hear the bowel sound after surgery1-5 days

    Defined as the first time flatus happens

  2. time to report of first defecation

    Time frame: End of surgery to the first defecation 1-7 days

    Defined as the first time defecation happens.

Secondary outcomes

  1. length of postoperative hospitalization

    Time frame: End of surgery to hospital discharge 5-7 days

    Defined as the length hospitalization after surgery

Sponsors and collaborators

Lead sponsor

Eskisehir Osmangazi University

Other

Registry information

Important dates

Study start
2019
Primary completion
2019
Study completion
2020
First posted
Jul 10, 2020
Registry last updated
Jul 10, 2020

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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