Exploring the Effects of a Baduanjin Program on the Symptoms of Constipation in Patients With Schizophrenia Spectrum

Sponsor
National Yang Ming University (Other)
Overall Status
Completed
CT.gov ID
NCT04071444
Collaborator
Tri-Service General Hospital (Other)
112
1
2
8.7
12.8

Study Details

Study Description

Brief Summary

Patients with schizophrenia spectrum have been suffering from constipation due to long-term use of psychotropic medications and changes in physical activity and eating habits caused by diseases.

Aim this study was to examine the effectiveness of Baduanjin program in improving the symptoms of intestinal peristalsis and constipation in patients with psychosis.

Method:A randomized controlled trial was conducted in tow psychiatric centers in northern Taiwan.The experimental group was provided with an 8- session Baduanjin program for 24 weeks (1 hour, thrice times per week), while the control group received routine care.

Condition or Disease Intervention/Treatment Phase
  • Other: Baduanjin program
N/A

Detailed Description

This study was conducted in two psychiatric center. Residents in one of psychiatric center were allowed to walk for 20 min after dinner every day, and each unit residents rare active. In this study, patients on the schizophrenia spectrum were invited to receive screening for constipation syndrome. A total of 275 patients agreed to undergo the screening. In total of 112 patients satisfied the inclusion criteria, and 58 patients consented to participate in the experiment.

Each participant was assigned one number from 1 to 112 by the first author. The second author enrolled participants. They were randomized to either Baduanjin program group or routine care group in a 1:1 ratio using blocked randomization having a block size of 3. Patients in the experimental group (EG) participated in the Baduanjin intervention in a privacy setting", which involved 60-min sessions 3 times per week, 1 hour after dinner between 6 and 7 pm; the entire program continued for 24 weeks. The control group (CG) received routine care. The outcome indicators for this intervention program involved the risk factors for constipation, constipation symptoms, and Intestinal Peristalsis.

Study Design

Study Type:
Interventional
Actual Enrollment :
112 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The participants were divided into experimental and control groups through block randomization.The participants were divided into experimental and control groups through block randomization.
Masking:
Single (Participant)
Masking Description:
The data of Intestinal Peristalsis in four quadrants were collected by a research assistant.
Primary Purpose:
Other
Official Title:
Exploring the Predictors of Constipation and the Effects of a Baduanjin Program on the Symptoms of Constipation in Adults With Chronic Schizophrenia
Actual Study Start Date :
Oct 8, 2018
Actual Primary Completion Date :
Jul 1, 2019
Actual Study Completion Date :
Jul 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Baduanjin program

The entire program continued for 6 months (December, 2018 to July, 2019), and the intervention was performed for 60 min 3 times per week; particular attention was paid to the disease characteristics of the patients with chronic schizophrenia and to preventing excessive fatigue. Every session began with a 20-min warm-up, followed by 20 min of Baduanjin program, and ended with a cool-down session. The participants were instructed, with the assistance of a video, to practice Baduanjin program in a group by two authors who are experienced in the psychiatric nurses and had been trained in this program.

Other: Baduanjin program
The entire program continued for 6 months (December, 2018 to July, 2019), and the intervention was performed for 60 min 3 times per week; particular attention was paid to the disease characteristics of the patients with chronic schizophrenia and to preventing excessive fatigue. Every session began with a 20-min warm-up, followed by 20 min of Baduanjin program, and ended with a cool-down session. The participants were instructed, with the assistance of a video, to practice Baduanjin program in a group by two authors who are experienced in the psychiatric nurses and had been trained in this program.

No Intervention: Control group

The control group (CG) received routine care.

Outcome Measures

Primary Outcome Measures

  1. Changes in Intestinal Peristalsis [3 months and 6 months]

    Change from Baseline bowel movement of four quadrants of abdomen at 3 months and 6 months

Secondary Outcome Measures

  1. Changes in Constipation Assessment Scale [3 months and 6 months]

    Change from Baseline Constipation Assessment Scale at 3 months and 6 months. The nine symptoms evaluated included: bloating, increased gas delivery in the rectum, decreased / increase frequency of bowel movements, oozing water, rectal obstruction or pressure, bowel movements combined with rectal pain, low bowel movements, and inability to defecate. 3 points scoring method (0-2), 0 is no problem, 1 is a bit problem, 2 is a serious problem. The maximum total score is 18.

  2. Change in Patient Assessment of Constipation Symptoms [3 months and 6 months]

    Change from Baseline Patient Assessment of Constipation Symptoms at 3 months and 6 months. The 12 items are divided into 3 subscales: 4 items for abdominal symptoms, 3 items for rectal symptoms, and 5 items for fecal symptoms. Patient Assessment of Constipation Symptoms Scale items are rated on a 5-point scale ranging from 0 to 4 based on severity of each item. The maximum total score is 48.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 64 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Comply with the diagnosis of the spectrum.

  • Have the willingness to participate in the study and could read, communicate and cooperate with the completion of the consent form and questionnaire.

  • The age is 20 to 64 years old.

  • No need for any assistance in walking, and the gait is stable.

  • Appeared more than 2 times in the past month for more than 3 consecutive days without resolving or routine use of laxatives

Exclusion Criteria:
  • Diagnosis is organic brain disease, alcohol and substance abuse.

  • There have been problems with gastrointestinal bleeding or lesions.

  • Have a history of extensive abdominal surgery or gastrointestinal surgery.

  • There are medical considerations and medical expenses reduction activities.

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Yang-Ming University Taipei City Taiwan

Sponsors and Collaborators

  • National Yang Ming University
  • Tri-Service General Hospital

Investigators

  • Principal Investigator: Chiu-Yueh Yang, PhD, Yang Ming National University
  • Study Director: Li-Ru Wang, MSN, National Yang Ming University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
National Yang Ming University
ClinicalTrials.gov Identifier:
NCT04071444
Other Study ID Numbers:
  • 2-107-05-114
First Posted:
Aug 28, 2019
Last Update Posted:
Sep 9, 2020
Last Verified:
Mar 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by National Yang Ming University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 9, 2020