Corestability Training in Overweight Children

Sponsor
Asir John Samuel (Other)
Overall Status
Completed
CT.gov ID
NCT04315220
Collaborator
Maharishi Markandeshwar International School (Other)
20
1
2
5.6
3.6

Study Details

Study Description

Brief Summary

A total of 52 overweight children aged between eight and sixteen years will be recruited by criterion based purposive sampling to participate in the two groups pretest post test randomized clinical study. Random allocation of the eligible subjects for treatment will be done by the block randomization method with matrix of thirteen rows and four columns (13x4). The subject will be allotted to the group randomly, based on the chit selected by the person other the primary researcher.Once the block is filled, the next row block will be opened. Thus equal distribution of overweight children in the each group will be ensured.

Group A will be receiving actual core stability training (Level 1 - Mat exercises and Level 2

  • Swiss Ball exercises) for 6 weeks with a frequency of three sessions per week.Group B will receive no training. Each session will last for 30 minutes of duration. The static and dynamic balance, foot pressure distribution and core strength will be assessed at the baseline and at the end of the treatment sessions.
Condition or Disease Intervention/Treatment Phase
  • Other: Corestability training
  • Other: No Intervention
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two group pre-test post-test designTwo group pre-test post-test design
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effectiveness of Core Stability Training in Improving Postural Stability and Foot Pressure Distribution in Overweight Children: A Randomized Controlled Trial
Actual Study Start Date :
Oct 13, 2020
Actual Primary Completion Date :
Feb 13, 2021
Actual Study Completion Date :
Mar 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group (Core stability training (CST))

Core stability training (CST) consists of two levels: level 1- Mat exercises (includes abdominal muscle contraction, bridging,cat stretch,single leg circle and superman) and level 2- Swiss ball exercises (includes abdominal muscle contraction, bridging and squatting by using therapy ball). There will be three sets of 15 repetitions of each exercises. The first set will consist of 10 seconds hold period, follow by 12 seconds hold in second set and 15 seconds hold in third set respectively. The entire session will last for approximately 30 minutes.

Other: Corestability training
Level -1: Mat exercises Abdominal muscle contraction,bridging,cat stretch,single limb circle and superman.: Level- 2: Swiss Ball Exercises Abdominal contraction,bridging and squats.

Active Comparator: Control group

Will not receive any kind of training.

Other: No Intervention
No Intervention

Outcome Measures

Primary Outcome Measures

  1. Foot pressure distribution [change from baseline and six weeks]

    All overweight children will be asked to walk barefoot along a 5-.metre walkway using Harris mat pressure distribution platform which will be placed on a firm, level surface, in the centre of walkway. Children will be ensured to step on the Harris mat without pause, first with one foot and then repeat the same procedure with the other foot at constant speed. Foot markings then analyzed by using

  2. Single limb stance [change from baseline and six weeks]

    The children will be instructed to stand on the dominant leg with non dominant leg flexed to 90 degree, and maintain the position. The test will be performed first with eyes open and then with the eyes closed. The time for which participant will be able to maintain balance will be recorded

  3. Y- reach set [change from baseline and six weeks]

    The participant will stand on one foot in the center of the Y with the most distal aspect of the toes just behind the starting line. While maintaining single-leg stance, the balance will be tested in the anterior, postero-medial and postero-lateral direction with reach foot. The reach distance in all the three directions will be noted.

  4. Core Strength [change from baseline and six weeks]

    The core strength will be measured with the Chattanooga Pressure Biofeedback Unit. The device will be placed under the lumbar spine in crook lying and inflated to a baseline of 40 mmHg. The participants will be instructed to perform drawing-in maneuver on the verbal instructions, maintain it for 10 sec. The change in pressure will be noted

Eligibility Criteria

Criteria

Ages Eligible for Study:
8 Years to 16 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Children of age 8- 16 years old.

  2. Both Boys and Girls.

  3. Child with BMI-for-age percentile growth between 85th to less than 95th percentile.

Exclusion Criteria:
  1. Uncooperative participants.

  2. Upper or lower limb fracture or injury in recent 6 months.

  3. Any musculoskeletal or neurological disorder affecting core strength and balance.

  4. Refuse to participate because not able to understand the researcher instructions.

  5. Unable to attend the whole sessions during the research period.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kanu Goyal Ambala Haryana India 133207

Sponsors and Collaborators

  • Asir John Samuel
  • Maharishi Markandeshwar International School

Investigators

  • Principal Investigator: Kanu Goyal, BPT, DOMTP, Maharishi Markandeshwar Institute of Physiotherapy and Rehabilitation
  • Study Chair: Asir J Samuel, MPT, PhD, Maharishi Markandeshwar Institute of Physiotherapy and Rehabilitation

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Asir John Samuel, Associate Professor, Maharishi Markendeswar University (Deemed to be University)
ClinicalTrials.gov Identifier:
NCT04315220
Other Study ID Numbers:
  • MMDU/2020
  • U1111-1249-8305
First Posted:
Mar 19, 2020
Last Update Posted:
Apr 15, 2021
Last Verified:
Apr 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Asir John Samuel, Associate Professor, Maharishi Markendeswar University (Deemed to be University)
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 15, 2021