- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05785416
Stretching Techniques of Knee Muscles and Their Effect on Joint Range, Suppleness and Muscle Activity in Elderly
March 24, 2023 updated by: Deepak Malhotra
Effects of Proprioceptive Neuromuscular Facilitation on Joint Range of Motion, Flexibility and Electromyographic Activity of Knee Muscles in Older Adults
The goal of this clinical trial was to compare the effect of two different types of stretching techniques in elderly population. The main questions it aims to answer are:
- What is the immediate effect (after a single intervention) of these stretching techniques on muscle flexibility, amount of knee joint motion and muscle activity?
- What is the effect of a four week intervention program of these stretching techniques on muscle flexibility, amount of knee joint motion and muscle activity? There were three groups with ten randomly allocated participants in each group. Intervention group I was given a stretching technique called contract-relax technique and the Intervention group II was given static stretching. The third group was not given any treatment and was taken as a control. The main aim was to find out that whether the two techniques are effective or not and which one of the two is better than the other in terms of improvement in the above mentioned parameters.
Study Overview
Status
Completed
Conditions
Detailed Description
The objective of the study was to compare the effects of Proprioceptive Neuromuscular Facilitation - Contract Relax (PNF- CR) and static stretch techniques immediately and post four weeks of intervention on knee range of motion, flexibility and electromyographic activity of knee muscles among older adults.
This is an outcome assessor-blinded pre-test post-test randomized controlled trial with two experimental groups (PNF-CR and Static Stretching) and a control group.
30 males aged 55-75 years were randomly assigned into PNF group (n=10), Static Stretch group (n=10) and Control group (n=10).
Knee range of motion, electromyographic activity of hamstrings and sit and reach test, were taken for the dominant side thrice: pre-intervention, immediately after stretching and after the training period.
Active knee range of motion (ROM) was assessed using a universal goniometer.
Surface Electromyography (EMG) was used to record Maximal voluntary isometric contraction (MVIC) of biceps femoris and the Chair Sit-and-Reach Test (CART) was used to assess the hamstring muscle's length flexibility.
Study Type
Interventional
Enrollment (Actual)
30
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
-
-
Delhi
-
New Delhi, Delhi, India, 110025
- Out Patient Department, Centre for Physiotherapy & Rehabilitation Sciences, Jamia Millia Islamia
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-
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
55 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Male adults aged between 55 and 75 years
- Able to do activities of daily living (ADL) without assistance
- Able to comprehend and follow instructions
Exclusion Criteria:
- Grade III or IV osteoarthritis or any other musculoskeletal condition affecting the muscle length.
- History of any surgery to hip, knee, low back or ankle
- History of any medication (anti-inflammatory, for pain relief, or anti-arthritic) in previous six months
- History of life-threatening disease (neurological disease, cardiovascular disease, severe hypertension)
- Passive full knee extension (popliteal angle 180 degrees)
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: PNF- CR Group
The participants in the group were given PNF contract- relax stretching using the standard protocol.
One trial had two isometric contractions each followed by five seconds muscle stretch and there was a total of four trials.
Total of 12 sessions in 4 weeks (3sessions/week).
|
PNF-CR utilized the concept of autogenic inhibition of the muscle for improving the flexibility of the muscle.
It includes stretching a muscle after a brief period of activation.
|
|
Experimental: Static Stretching Group
The participants in the group were given sustained stretching for a period of 80s at a stretch. Total of 12 sessions in 4 weeks (3sessions/week). |
The SS technique utilized the concept of creep for improving the hamstring flexibility.
The stretch was maintained for a prolonged period passively by the therapist.
|
|
No Intervention: Control Group
No intervention was given in this group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Active Knee Range of Motion
Time Frame: Baseline, After 1st intervention (immediate), 4 weeks after intervention
|
The active extension knee range of motion was measured using a universal goniometer.
|
Baseline, After 1st intervention (immediate), 4 weeks after intervention
|
|
Change in Maximum Voluntary Isometric Contraction (MVIC)
Time Frame: Baseline, After 1st intervention (immediate), 4 weeks after intervention
|
The Electromyographic activity of the biceps femoris muscle was evaluated using the surface electrodes during the maximal isometric contraction.
|
Baseline, After 1st intervention (immediate), 4 weeks after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Hamstring flexibility
Time Frame: Baseline, After 1st intervention (immediate), 4 weeks after intervention
|
The hamstring flexibility was measured using the Chair Sit and Reach Test (CART)
|
Baseline, After 1st intervention (immediate), 4 weeks after intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Sahar Zaidi, MPT, Jamia Millia Islamia
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)
March 1, 2018
Primary Completion (Actual)
November 28, 2018
Study Completion (Actual)
January 24, 2019
Study Registration Dates
First Submitted
March 13, 2023
First Submitted That Met QC Criteria
March 24, 2023
First Posted (Actual)
March 27, 2023
Study Record Updates
Last Update Posted (Actual)
March 27, 2023
Last Update Submitted That Met QC Criteria
March 24, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 16/9/121/JMI/IEC/2017
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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