Clinical Trial: Effect of Transcutaneous Electrical Stimulation on Constipation

Study Status: RECRUITING
Recruit Status: RECRUITING
Study Type: INTERVENTIONAL




Official Title: Effects of Transcutaneous Electrical Nerve Stimulation on Constipation in Children With Cerebral Palsy

Brief Summary:

Cerebral palsy (CP) is a group of non-progressive neurological disorders that affect body movement, muscle coordination, and posture .It is caused by damage in developing brain, usually before or during birth, but can also occur during early childhood.
They may include muscle stiffness or floppiness, abnormal reflexes, impaired coordination, difficulty with fine motor skills, speech and swallowing difficulties, involuntary movements, problems with balance and posture, and intellectual or developmental disabilities.
Constipation is a common gastrointestinal issue in children with cerebral palsy (CP) due to reduced muscle tone, impaired coordination, limited mobility, and side effects of certain drugs like antispasmodics or anti-epileptics.
Transcutaneous electrical nerve stimulation (TENS) is a non-invasive therapy.
Usually, TENS is commonly used as pain management modality, its role in treating constipation in children with cerebral palsy is still being explored.
Research on the use of TENS for constipation in children with cerebral palsy is limited, and most studies have focused on constipation in adults or individuals without CP.
However, some studies have investigated the effects of TENS on gastrointestinal function in children with CP, including constipation.

This study was Randomized Controlled Trial with random sampling technique.
Study was conducted in DHQ Hospital, Hafizabad from July 2023 to December 2023 on 34 children with cerebral palsy with constipation having age from 1 to 6 years according to inclusion and exclusion criteria.
After recruitment, it was divided into two Groups.
Baseline treatment was provided to control group while TENS will be used in other experimental group.
TENS was applied on abdominal area for 20 minutes along with baseline treatment.
Record pre and post session history of patient defecation frequency per week, abdominal pain or discomfort, and type of stool via using Rome-IV criteria, Bristol Stool Scale, Constipation Assessment scale and Gross Motor Function Classification System before and after treatment.
Data Analyses was based on statistical parameters and comparison performed before and after application of treatment.