None listed
Conditions
Interventions
Others(healthcare device) : Application time: 30 minutes per day
- Control group: self-massage 30 minutes,
- Training group 1: 30 minutes of vibration program
- Training group 2: 15 minutes of vibrati
Sponsors
Jeonbuk National University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 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
Exclusion criteria
Exclusion criteria: 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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| constipation severity index | — |
Secondary
| Measure | Time frame |
|---|---|
| Colon transit time;HRQOL(SF-36) | — |
Countries
Korea, Republic of
Contacts
Public ContactSeung-Rok Kang
Jeonbuk National University Hospital
Outcome results
None listed