- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04045106
The Acute Effect of Proprioceptive Neuromuscular Facilitation on Cervical Range of Motion, Strength and Proprioception. (RCT)
The Acute Effect of Proprioceptive Neuromuscular Facilitation on Cervical Range of Motion, Strength and Proprioception
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Istanbul
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Beşiktaş, Istanbul, Turkey, 34353
- Bahçeşehir University
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İstanbul
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Ataşehir, İstanbul, Turkey, 34755
- Yeditepe University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Neck disability index score of 5 or less
- Able to understand and follow instructions
- Above 18 years old
Exclusion Criteria:
- Cervical trauma
- History of cervical inter-vertebral disc pathology
- Rheumatic diseases
- Whiplash syndrome
- History of surgeries to the neck, face and shoulders
- History of systemic diseases
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: PNF pattern
PNF patterns were performed using Dynamic of reversals technique which is characterized as active motion alternating from one direction (agonist) to the opposite (antagonist) without relaxing. The cervical patterns consisted of
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The participants were asked to sit on a chair, the therapist performed the pattern of movement himself then passively applied the pattern on the participant then asked the participant to perform the pattern, and the therapist observed and corrected the movement if it was done improperly.Then participants were told that the therapist will resist their movement, they were also told to keep breathing normally and to report any discomfort and/or pain.After mastering the pattern,the therapist placed one hand on the participant's mandibular and the other hand approximately between parietal and occipital bones to apply resistance through out the ROM, each pattern performed for 3 sets of 10 repetitions with 1-2-minute rest between sets.
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Experimental: PNF stretching
PNF stretching was done using contract-relax-antagonist contract (CRAC) technique for cervical flexors, extensors, right and left lateral flexors, right rotators and left rotators.
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was done for 6 repetitions with hold for 6 seconds in position of stretch and sub maximal isometric contraction for 6 seconds, 1-2-minute rest was given before changing the target muscle group
|
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Sham Comparator: control
Participants allocated to the control group received ineffective passive ROM.
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ineffective passive ROM for 10 repetitions for flexion, extension, right and left side bending and right and left rotation, it was done from neutral position to the limit of motion without causing any stretch to the muscle.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cervical Proprioception: Joint position accuracy method using cervical range of motion instrument.
Time Frame: 1 day
|
Joint position accuracy method using cervical range of motion instrument.
Participants were asked to sit and put on the CROM instrument, then they were instructed to start moving their head to one of directions then the assessor stopped them at 30 degrees and told them to feel the amount of movement and muscle tension, this was repeated 3 times as a reference, then they were asked to do the movement with the eyes closed until they reach the target angle, this was repeated for 3 times, this was done for each direction and the assessor recorded the results.
Cervical proprioception was done for flexion, extension, right side bending, left side bending, right and left rotation
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Range Of Motion
Time Frame: 1 day
|
Active Range of motion (AROM) was measured using cervical range of motion instrument. CROM instrument were placed on the participants head, then the assessor asked the participant to move towards the movement direction until they reach the limit. |
1 day
|
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Muscle strength
Time Frame: 1 day
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The measurement were taken for cervical flexors, extensors, right and left rotators, right and left side benders, each was done in an against gravity position.
|
1 day
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: SULE DEMIRBASISTANBUL, Yeditepe University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 10269393
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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