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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05719636
Other study ID # REC/RCR & AHS/22/0740
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 13, 2022
Est. completion date April 20, 2023

Study information

Verified date December 2023
Source Riphah International University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this research the effects of progressive resistance exercise training on endurance and functional mobility in children with spina bifida are assessed.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 20, 2023
Est. primary completion date April 15, 2023
Accepts healthy volunteers No
Gender All
Age group 8 Years to 16 Years
Eligibility Inclusion Criteria: - 8 to 16 year. - Male and female both are included. - Lower extremity weakness (less than 2). - Knee and hip flexion contractures Exclusion Criteria: - Bowel and bladder dysfunction. - Children having absent tone. - Children having bone fracture

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Conventional treatment
Conventional protocol that involves simple active and passive range of motion exercises of lower limb with positioning for assistive devices was provided
Progressive resistance exercise
The protocol that was applied on the members of (experimental group) are progressive resistance exercises. These passive resistance exercises included Flexion, Extension, Abduction, Adduction of hip; Flexion, Extension of knee; with minimum time in start and minimum quantity of loads, with Thera bands and sandbags,.

Locations

Country Name City State
Pakistan Children hospital Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient Specific Functional Scale for lower extremity functional status Patient Specific Functional Scale (PSFS) was developed by Stratford et al 1995 as a self-report outcome measure of function that could be used in patients with varying levels of independence. The aim of PSFS is to provide clinicians with a valid, reliable, responsive and efficient outcome measure that would be easy to use and applicable to a large number of clinical presentations. Gives the patient positive re-enforcement that the intervention is effective. Can be used on a wide variety of musculoskeletal and neurological conditions 6th week
Secondary 6 minute walk test The 6 Minute Walk Test is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity. 6th week
Secondary sit to stand test The participant is encouraged to complete as many full stands as possible within 30 seconds. The participant is instructed to fully sit between each stand. While monitoring the participant's performance to ensure proper form, the tester silently counts the completion of each correct stand 6th Week
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