Effects of Sensory Motor Training on Balance and Proprioception Among Post-Menopausal Obese Women

March 29, 2021 updated by: Riphah International University

Postmenopausal obese women often have difficulties with balance and proprioception. Sensorimotor training is an important part of physical therapy interventions, with emerging evidence that it could be beneficial for postmenopausal obese women.

Objective: To find the impact of sensorimotor training on balance and proprioception among postmenopausal obese women.

Study Overview

Detailed Description

Randomized clinical trial was conducted on postmenopausal obese women population with impaired balance and proprioception on inclusion & exclusion criteria, sample size of 40, ages ranged from 45 to 65 years included. Group A received SMT and Group B received CT. The interval of treatment was 6 weeks. Data is collected from THQ Samundri. FRT, TUG, OLS utilized to assess the pre-and post-estimations of postural strength.

Study Type

Interventional

Enrollment (Actual)

44

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan, 54000
        • Binash afzal

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

45 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • • Post-menopausal obese women

    • BMI ≥30
    • Participants independent in ADLs
    • self-ambulatory
    • healthy (having no known condition in which sensorimotor exercises would be contraindicated.)

Exclusion Criteria:

  • • History of ankle sprain

    • Uncontrolled diabetes mullites
    • Presence of orthopaedic problems.
    • Neurological disorders.
    • Psychological problems.
    • Cognitive issues.
    • People with severe visual issues

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group
Sensorimotor training exercises include wall slides , core exercises (Planks, leg raises, crunches, bridging) balance exercises (single leg side lift, leg lift with dumble, balance on stability ball) on unstable surface for 50-60 min (3 sets of 10 rep) of exercises and gait training (different patterns of walking).
Sensorimotor training exercises include wall slides , core exercises (Planks, leg raises, crunches, bridging) balance exercises (single leg side lift, leg lift with dumble, balance on stability ball) on unstable surface for 50-60 min (3 sets of 10 rep) of exercises and gait training (different patterns of walking
Active Comparator: Control group
Cut back on high-fat foods. Drink plenty of water Use sugar and salt in moderation. Eat fruits and vegetables Get enough calcium Pump up your iron. Get enough fiber
Cut back on high-fat foods. Drink plenty of water Use sugar and salt in moderation. Eat fruits and vegetables Get enough calcium Pump up your iron. Get enough fiber

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Functional Reach Test (FRT)
Time Frame: 2 months
Functional Reach Test (FRT) is a clinical outcome measure used to asses dynamic balance in one simple task.
2 months
Time Up and Go Test (TUG)
Time Frame: 2 months
Time Up and Go test is used to assess the individual's mobility, static and dynamic balance walking ability and risk of fall among older adults. Intratester and intertester reliability (ICC) in elderly populations
2 months
One Leg Stance Test (OLS)
Time Frame: 2 months
The Single leg Stance (SLS) Test is used to evaluate static postural and balance control with one eye open and standing on one leg
2 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 15, 2020

Primary Completion (Actual)

October 20, 2020

Study Completion (Actual)

December 20, 2020

Study Registration Dates

First Submitted

March 26, 2021

First Submitted That Met QC Criteria

March 26, 2021

First Posted (Actual)

March 29, 2021

Study Record Updates

Last Update Posted (Actual)

March 30, 2021

Last Update Submitted That Met QC Criteria

March 29, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • REC/Lhr/20/2050 Sehar Shabeer

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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