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Effect of 6 Weeks of Whole-body Vibration in Treatment of Postnatal Constipation

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Constipation

Treatments

Combination Product: Whole Body Vibration
Other: pelvic floor exercises and static abdominal exercises in addition to diet instructions

Study type

Interventional

Funder types

Other

Identifiers

NCT05286476
/012/002926

Details and patient eligibility

About

Background: Postpartum constipation is a common problem affecting postpartum mothers. Aim: To determine whether Whole Body Vibration is effective in treatment of postnatal women constipation. Design: The study was designed as a prospective, randomized, single-blind, pre-post-test, controlled trial.

HYPOTHESES:

It will be hypothesized that:

It was hypothesized that whole-body vibration has no or limited effect in treatment of postnatal constipation RESEARCH QUESTION: Does whole-body vibration has an effect in treatment of postnatal constipation?

Full description

Methods: Group A received whole-body vibration, pelvic floor exercise and static abdominal exercises interventions for six weeks and group B received pelvic floor exercises and static abdominal exercises in addition to diet instructions in both groups. Constipation symptom questionnaire and patient assessment of constipation quality of life questionnaire is applied before and after treatment.

Enrollment

40 patients

Sex

Female

Ages

22 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The participants age ranged from 22 to 35 years old
  • with vaginal delivery
  • complain from postnatal constipation from (2 - 6 weeks) post-delivery
  • had body mass index (BMI) ranged from 30 to 32 kg/m2.

Exclusion criteria

Participants were excluded if they:

  • had diabetes, hypertension, cardiac diseases.
  • Women who had history of inflammatory bowel disease and abnormalities of anal region or anal fissure
  • women who had history of bowel surgery (other than appendectomy),
  • patients who had endocrine disease or digestive tract disease
  • history of neurological or musculoskeletal disorder.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups

group A
Experimental group
Description:
received Whole-body Vibration, pelvic floor exercise and static abdominal exercises interventions In addition to diet instructions
Treatment:
Combination Product: Whole Body Vibration
Other: pelvic floor exercises and static abdominal exercises in addition to diet instructions
group B
Other group
Description:
received pelvic floor exercises and static abdominal exercises in addition to diet instructions only
Treatment:
Other: pelvic floor exercises and static abdominal exercises in addition to diet instructions

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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