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Whole-Body Vibration for Functional Constipation

C

Changhua Christian Medical Foundation

Status

Completed

Conditions

Constipation

Treatments

Procedure: whole body vibration

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

  1. Aim: The aim of this trial was to determine whether whole-body vibration (WBV) induced via a non-invasive oscillation platform could improve symptoms and health-related quality of life (HRQOL) in patients with chronic functional constipation.
  2. Methods: A single-blinded, randomized, control trial was performed in a single Hospital in Taiwan. Patients diagnosed with chronic functional constipation, as per the Rome III diagnostic criteria were included and randomized to either the WBV treatment or no treatment (control) group. The treatment group received six 15-minute sessions of WBV therapy over a two-week period. Patients received vibrations of 2 mm in amplitude at a frequency of 12 Hz. The primary outcome was assessed by the constipation severity instrument (CSI). The secondary outcome was improvements in HRQOL.

Enrollment

26 patients

Sex

All

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • met the Rome III criteria of constipation

Exclusion criteria

  • pregnant
  • cardiovascular disease
  • cerebrovascular disease
  • recently undergone major surgery
  • hypothyroidism
  • depressive disorder.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

26 participants in 2 patient groups, including a placebo group

vibration
Experimental group
Treatment:
Procedure: whole body vibration
placebo
Placebo Comparator group
Treatment:
Procedure: whole body vibration

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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