- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03767413
The Effects of Mental Practice Combined With Proprioceptive Neuromuscular Facilitation on Muscle Strength of Upper Limb and Hand Grip
May 15, 2019 updated by: Wafaa Mahmoud Amin, University of Jazan
Influence of mental practice and proprioceptive neuromuscular facilitation on muscle strength of upper limb and hand grip will be measured in 30 to 50 healthy students with right dominant hand, Their age will be ranged from 18 to 26 years old.
Subjects will randomly assigned to either proprioceptive neuromuscular facilitation (PNF) group or proprioceptive neuromuscular facilitation with mental practice (PNFMP) group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
PNF group: 15 - 25 individuals, these subjects will receive only PNF training.
PNFMP: 15 individuals, these subjects will receive PNF training with MP.
Training program will be conducted for every group for 5 weeks with 3 sessions x 30 min per week.
Electromyography (EMG) device will be used to measure the electrical activity of muscles using surface electrodes.
Hydraulic hand dynamometer will be used to measure hand grip strength.
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
-
-
Jazan
-
Riyadh, Jazan, Saudi Arabia, 45142
- Jazan University
-
-
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
18 years to 26 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- The participant will be right-handed.
- Previously untrained subjects.
- Absence of a prior injury of the hand or arm
Exclusion Criteria:
- History of a neurological disease.
- History of musculoskeletal injury of upper limb.
- Unstable medical condition
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: PNF group
It will be consisted of 15 -25 healthy subjects receiving only proprioceptive nueromuscular facilitation training for 5 weeks with 17 days follow up after completion of program.
|
proprioceptive neuromuscular facilitation training
|
Experimental: PNFMP
It will be consisted of 15 -25 healthy subjects receiving proprioceptive nueromuscular facilitation training and mental practice technique for 5 weeks with 17 days follow up after completion of program.
|
proprioceptive neuromuscular facilitation training and mental practice technique
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Shoulder joint strength
Time Frame: 6 minutes
|
electromyography device will be used to measure the electrical activity of the muscle
|
6 minutes
|
Elbow joint strength
Time Frame: 6 minutes
|
electromyography device will be used to measure the electrical activity of the muscle
|
6 minutes
|
Strength of hand grip
Time Frame: 15 minutes
|
Hand held dynamometer will be used to measure the strength of the hand grip
|
15 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
December 16, 2018
Primary Completion (Actual)
February 3, 2019
Study Completion (Actual)
February 10, 2019
Study Registration Dates
First Submitted
December 5, 2018
First Submitted That Met QC Criteria
December 5, 2018
First Posted (Actual)
December 6, 2018
Study Record Updates
Last Update Posted (Actual)
May 17, 2019
Last Update Submitted That Met QC Criteria
May 15, 2019
Last Verified
May 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 8810025277
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
there is no plan
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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