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Clinical Trials/NCT04661202
NCT04661202
Completed
Not Applicable

Effects of Exercise Training on Pelvic Floor Symptoms and Function in Adults With Constipation: A Randomized Controlled Trial

National Cheng Kung University1 site in 1 country27 target enrollmentJanuary 1, 2021
ConditionsConstipation

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Constipation
Sponsor
National Cheng Kung University
Enrollment
27
Locations
1
Primary Endpoint
Constipation Symptom-Time Spent During Defecation
Status
Completed
Last Updated
last year

Overview

Brief Summary

Constipation is a common problem in the general population. Defecation disorders caused by abnormal contraction or insufficient relaxation of the pelvic floor muscles during defecation may be one of the most possible causes of constipation. Although constipation is not life-threatening, it may have a significant impact on the quality of life. Aerobic exercise has been shown to improve symptoms of constipation in adults with constipation. However, there is no research investigating the effects of a multimodal exercise training on pelvic floor symptoms and pelvic floor muscle function in this population and only few studies have evaluated the pelvic floor muscle function using objective assessment tools among this population. The aim of the study is to investigate the effect of a multimodal exercise training program on constipation symptoms and pelvic floor muscle function in adults with constipation. The investigator will conduct a randomized controlled trial to evaluate the effectiveness of exercise training for adults with constipation. This study hypothesizes that (1) a multimodal exercise training can improve pelvic floor symptoms and function in adults with constipation, and (2) the improvement in exercise training group will be higher than that in control group.

Detailed Description

This is a randomized controlled trial. Adults with constipation will be recruited and randomly assigned to either the intervention group or the control group. The intervention group will receive 16 sessions of therapist-supervised, combined resistance (including pelvic floor muscle training) and aerobic exercise training twice weekly for 8 weeks. The control group will receive usual care. All participants will be assessed at baseline and post-intervention. The primary outcome measure is the severity of the patient's self-reported constipation symptoms measured using the Patient Assessment of Constipation Symptoms Questionnaire (PACSYM). The secondary outcomes are pelvic floor muscle function assessed through the Pelvic Floor Muscle Coordination Scale (PFMCS), digital rectal examination, and anorectal manometry; quality of life measured by the Patient Assessment of Constipation Quality of Life Questionnaire (PACQOL); and physical activity levels measured using the International Physical Activity Questionnaire (IPAQ). Intention-to-treat analysis will be performed to preserve the sample size and original randomization. Mann-Whitneyand Chi-square testsest will be used for continuota and categorical data to compare the baseline characteristics between the two groups. Wilcoxon signed-rank test and the Mann-Whitney U test will be used for intragroup and intergroup comparison of outcome variables. The p-value of \< 0.05 will be considered statistically significant.

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
July 31, 2022
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kuan-Yin Lin

Assistant professor

National Cheng Kung University

Eligibility Criteria

Inclusion Criteria

  • Aged between 20 years and 64 years
  • Participants who fulfill the Rome IV criteria for constipation which include two or more of the following: a) straining \> 25% of defecations; b) lumpy or hard stools \> 25% of defecations; c) sensation of incomplete evacuation \> 25% of defecations; d) sensation of anorectal obstruction/blockage \> 25% of defecations; e) manual maneuvers to facilitate \> 25% of defecations; f) \< 3 spontaneous bowel movements per week
  • Participants who have sufficient language skills to participate

Exclusion Criteria

  • Participants who have received exercise or pelvic floor muscle training under supervision in the past 12 months
  • Participants with previous abdominal surgery, anorectal trauma or surgery, or previous diagnosis of neuropathy or anal sphincter dysfunction
  • Presence of malignancies, severe cardiovascular disease or other severe physical/psychiatric impairments that prevent participation in the study
  • Pregnant or within 12 months postpartum

Outcomes

Primary Outcomes

Constipation Symptom-Time Spent During Defecation

Time Frame: absolute values at 8 weeks

A Seven Day Bowel Diary includes items regarding time spent during defecation.

Severity of Constipation Symptoms

Time Frame: absolute values at 8 weeks

The Patient Assessment of Constipation Symptoms questionnaire will be used to assess the severity of constipation symptoms. This questionnaire includes a total of 12 items in 3 subscales: abdominal (4 items), rectal (3 items), and stool (5 items). Participant will be asked to rank the symptoms on a five-point Likert scale, ranging from 0 (absent) to 4 (very severe). The total score ranges from 0 to 48 which will be divided by the actual number of items answered. The higher score indicates the greater severity of constipation symptoms.

Constipation Symptoms

Time Frame: absolute values at 8 weeks

A Seven Day Bowel Diary includes items regarding the stool frequency, presence of incontinence, excessive straining, manual maneuver, or pain during defecation, and the use of laxatives.

Constipation Symptom-Stool Consistency

Time Frame: absolute values at 8 weeks

A Seven Day Bowel Diary includes the item regarding stool consistency. The Bristol Stool Form Scale describing the shapes and types of stools is used to evaluate stool consistency. This scale assigns a number (1-7) with 1 indicating hardest to 7 indicating loosest, to classify human feces based on its shape and and how formed or loose it is.

Secondary Outcomes

  • The Pelvic Floor Muscle Coordination Measured by the Pelvic Floor Muscle Coordination Scale(absolute values at 8 weeks)
  • Constipation Quality of Life(absolute values at 8 weeks)
  • The Pelvic Floor Muscle Strength Will be Measured by Digital Rectal Examination.(absolute values at 8 weeks)
  • The Pelvic Floor Muscle Function Will be Measured Using Anorectal Manometry.(absolute values at 8 weeks)
  • The Pelvic Floor Muscle Endurance Will be Measured Using Anorectal Manometry and Stopwatch.(absolute values at 8 weeks)
  • Physical Activity Levels(absolute values at 8 weeks)
  • Adherence(absolute values at 8 weeks)

Study Sites (1)

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