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A comparative study of the effect of Kegel exercises and conventional therapy vs in treating functional constipation in children

A comparative study of the effect of Kegel exercises and conventional therapy vs in treating functional constipation in children

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230424057984N1
Enrollment
64
Registered
2023-05-08
Start date
2022-03-21
Completion date
Unknown
Last updated
2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

functional constipation. Constipation

Interventions

Intervention 1: Control group: Control group: The basic treatment including diet training, defecation training and polyethylene glycol syrup was used. In this way, 0.7 g/kg of polyethylene glycol syru

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 18 Years

Inclusion criteria

Inclusion criteria: • Age 8 to 18 years Willingness to participate Parent(s) sign the informed consent Functional constipation according to Rome Iv

Exclusion criteria

Exclusion criteria: Severe delay in motor skills development Constipation caused by medicine Bowel surgery (except appendectomy) Endocrine and metabolic disorders (hypothyroidism, hypercalcemia, diabetes mellitus, diabetes insipidus) Neurological and psychiatric disorders (spina bifida, cerebral palsy, anorexia nervosa, autism, or PDD-NOS) Down syndrome Hirschsprung's disease

Design outcomes

Primary

MeasureTime frame
Frequency of defecation. Timepoint: At the beginning of the study (before the start of the intervention) then 3 months later. Method of measurement: Likert scale: 2 times a week, once a week, less than once a week, less than once a month.;Duration of defecation. Timepoint: At the beginning of the study (before the start of the intervention) then 3 months later. Method of measurement: Likert scale: less than 5 minutes, 5-10 minutes, 10-20 minutes.;Incomplete evacuation of stool. Timepoint: At the beginning of the study (before the start of the intervention) then 3 months later. Method of measurement: Likert scale: never, rarely, sometimes, usually.;Abdominal pain. Timepoint: At the beginning of the study (before the start of the intervention) then 3 months later. Method of measurement: Likert scale: never, rarely, sometimes, usually.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Hadi Imaniyeh

Shiraz University of Medical Sciences

imaniehm@sums.ac.ir+98 917 111 0674

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026