Effects of Compelled Body Weight Shift Technique for Rehabilitation of Individuals With Chronic Stroke

September 1, 2020 updated by: Usman Farooq, Northwest Institute of Health Sciences, Pakistan
Stroke is one of the major cause of lifelong disability if not treated on time, the investigator's technique knows as Compelled Body Weight Shift Technique (CBWS) was utilized and administered to chronic stroke population and results were figured out using gait parameters and Tinetti POMA scale.

Study Overview

Detailed Description

Total 28 sample size out of which 27 were divided into control and experimental group. Inclusion criteria was Unilateral chronic stroke with asymmetrical stance, Patients with score of 3,4 and 5 will be included according to FAS (Functional Ambulation Scale), Ability to understand and follow instructions, Both male and female, Any type of stroke, and Age 40-60. Written and informed consent was obtained from participants of study. Six weeks of exercise training was combined with compelled body weight shift technique via shoe lift of 0.6 cm thickness for experimental group and for control group training was performed without shoe lift.

Study Type

Interventional

Enrollment (Actual)

27

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

    • KP
      • Peshawar, KP, Pakistan, 25000
        • Usman Farooq, Mspt

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

40 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Unilateral chronic stroke with asymmetrical stance
  • Patients with score of 3,4 and 5 were included according to functional ambulation scale(59)
  • Ability to understand and follow instruction
  • Both male and female.
  • Any type of stroke.
  • Age 40-60.

Exclusion Criteria:

  • • Serious or unstable medical, condition of patient.

    • History of other neurological diseases (i.e. Parkinson's disease, multiple sclerosis),
    • Contractures or any deformity.
    • Leg Length Discrepancy

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental Group (Group A)

Subjects were randomly assigned and informed consent was obtained, the subjects were educated about treatment and on the basis of functional ambulation scale 3,4 and 5 subjects were included, along with this the subjects of age group between 40-60 having ability to understand and follow instructions were included in study.

Results were obtained by using gait parameters including walk speed, cadence, step rate, stride length The tinetti POMA scale was utilized to record changes post treatment in gait , the weight bearing was recorded using Camry ZT-160 analog weight scale At the end of every week results were obtained.

Routine Physical Therapy with 0.6 cm thickness insole inserted in shoe of unaffected side and following exercises were performed by patients

  • Muscle re-education
  • Sit to stand exercise , 4 to 10 repetitions
  • Supported heel raise to 10 repetitions with 3 sets
  • Supported squat exercise tibialis anterior and quads muscles to 10 repetitions with 3 sets
  • Gait training
  • Forward walk in parallel bars with number of 10 rounds.
  • Task oriented training balance training
  • A. Stepping exercise on 15 cm height step and number of repetitions 10.
  • B. Tandem standing for 10 seconds.
  • C. Reaching exercise in which patient performed reaching for object in therapists hand and the number of repetitions was 10.
Other: Control group: (Group B)

Subjects were randomly assigned and informed consent was obtained, the subjects were educated about treatment and on the basis of functional ambulation scale 3,4 and 5 subjects were included, along with this the subjects of age group between 40-60 having ability to understand and follow instructions were included in study.

Results were obtained by using gait parameters including walk speed, cadence, step rate, stride length The tinetti POMA scale was utilized to record changes post treatment in gait , the weight bearing was recorded using Camry ZT-160 analog weight scale At the end of every week results were obtained.

Routine Physical Therapy without 0.6 cm thickness insole inserted in shoe of unaffected side and following exercises were performed by patients

  • Muscle re-education
  • Sit to stand exercise , 4 to 10 repetitions
  • Supported heel raise to 10 repetitions with 3 sets
  • Supported squat exercise tibialis anterior and quads muscles to 10 repetitions with 3 sets
  • Gait training
  • Forward walk in parallel bars with number of 10 rounds.
  • Task oriented training balance training
  • A. Stepping exercise on 15 cm height step and number of repetitions 10.
  • B. Tandem standing for 10 seconds.
  • C. Reaching exercise in which patient performed reaching for object in therapists hand and the number of repetitions was 10.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Tinetti Performance Oriented Mobility Assessment
Time Frame: upto 6 weeks

Tinetti Performance Oriented Mobility Assessment The Tinetti, evaluation instrument is, an effectively managed, task-arranged test that, quantifies gait and balance activities of patients. A three-point, ordinal scale, extending from 0-2. "0" demonstrates the most elevated level of debilitation and "2" the people's freedom.

  1. Total Balance Score = 16
  2. Total Gait Score = 12
  3. Maximum total test Score = 28 [Time Frame: upto 6 weeks]
upto 6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
A 10meter walk test
Time Frame: upto 6 weeks
A 10meter walk test A ten meter distance employed, to determine functional mobility and gait speed, the ten meter walk test was performed by patient at self-selected walking pace and fast walking pace
upto 6 weeks
Camry 160 Analog Weight Scale
Time Frame: upto 6 weeks
Camry 160 Analog Weight Scale to check the weight in kilograms
upto 6 weeks

Collaborators and Investigators

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

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)

July 12, 2020

Primary Completion (Actual)

August 29, 2020

Study Completion (Actual)

August 31, 2020

Study Registration Dates

First Submitted

July 16, 2020

First Submitted That Met QC Criteria

July 20, 2020

First Posted (Actual)

July 21, 2020

Study Record Updates

Last Update Posted (Actual)

September 2, 2020

Last Update Submitted That Met QC Criteria

September 1, 2020

Last Verified

September 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

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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