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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT06444932
Other study ID # FUI/CTR/2024/12
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date June 10, 2024
Est. completion date December 30, 2024

Study information

Verified date June 2024
Source Foundation University Islamabad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Joint mobilization and resistance exercise training are effective conservative treatment options for the management of osteoarthritis. However, currently no study has highlighted the supplementary effects of resistance training in addition to joint mobilization in people suffering from knee osteoarthritis. The current study is aimed at bridging the gap in literature and providing evidence regarding the additive impact of resistance training to joint mobilization in knee osteoarthritis.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 44
Est. completion date December 30, 2024
Est. primary completion date December 10, 2024
Accepts healthy volunteers No
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria: - Knee OA grade I-III - Individuals of either gender aged 40-70 years - Knee OA history of no less than 3 months - Knee pain no more than 8/10 cm on the visual analogue scale (VAS) - Radiological evidence of grade III or less on Kellgren classification. Exclusion Criteria: - Those with signs of serious pathology such as malignancy, inflammatory disorder or infection. - History of trauma or fractures in lower extremity - Signs of lumbar radiculopathy or myelopathy - History of knee surgery or replacement and/or receiving intra-articular steroid therapy in the preceding two months

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Joint Mobilization
Patellofemoral and tibiofemoral joint mobilization
Resistance Exercise Training
Lower limb resistance exercise training
Device:
Transcutaneous Electric Nerve Stimulation (TENS)
Transcutaneous Electric Nerve Stimulation (TENS)
Heating Pad
Heating pad for heat therapy

Locations

Country Name City State
Pakistan Foundation Univeristy Islamabad Islamabad

Sponsors (1)

Lead Sponsor Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Walking related performance fatigability Walking related performance fatigability will be measured using 6 minute walk test. Greater fatigability indicates poorer outcome. 4 weeks
Primary Stride Length Gait analysis will be done to analyze stride length. A greater stride length signifies positive outcome and prognosis. 4 weeks
Primary Gait velocity Gait analysis will be done to analyze gaot velocity. A greater gait velocity signifies positive outcome and prognosis. 4 weeks
Primary Knee Pain Knee Pain will be measured using visual analogue scale (VAS) from 0-100mm. A higher score on VAS indicated greater pain. 4 weeks
Primary Knee range of motion Knee range of motion will be measured using a goniometer. A higher ROM signifies positive outcome. 4 weeks
Primary Functional Disability Knee functional disability will be assessed using Knee Osteoarthritis and Outcome Score (KOOS) with a score ranging from 0-100. A lower score on KOOS signifies greater functional disability. 4 weeks
Primary Isometric Muscle Strength Isometric Muscle Strength will be quantified using dynamometer. A higher score on dynamometer signifies greater muscle strength and good prognosis. 4 weeks
Primary Functional capacity 5 repetition sit to stand test will be used to determine knee related functional capacity, which will be quantified in terms of time. A smaller time will denote greater functional capacity. 4 weeks
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