A single-institution, open, exploratory clinical trial to evaluate the effect of whole-body vibration stimulation treatment on the improvement of bowel function using a sonic whole-body vibrator (SW-VMPROTM) for adults men and women with functional constipation over 20 years of age
- Conditions
- Diseases of the digestive system
- Registration Number
- KCT0006457
- Lead Sponsor
- Jeonbuk National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
1) Adult male and female over 20 years of age
2) Those who have had 2 or more of the 6 symptoms presented in the Rome IV constipation assessment criteria for more than 3 months
3) A person who has no communication problems in carrying out and proceeding with the clinical trial
4) A person who fully understands the research purpose and procedure and wishes to participate in clinical research through voluntary consent
1) Those who do not meet the age criteria
2) Those who have had gastrointestinal surgery within the last 6 months
3) Those with gastrointestinal bleeding, obstructive lesions and open wounds in the abdomen
4) Those who have been taking constipation relievers for 1 month before
5) Those who have dizziness against vibration
6) Pregnant and lactating women
7) Others recognized by the principal investigator as inappropriate to participate in the study
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method constipation severity index
- Secondary Outcome Measures
Name Time Method Colon transit time;HRQOL(SF-36)