RCT: The Acute Effect of Proprioceptive Neuromuscular Facilitation on Cervical Range of Motion, Strength and Proprioception.

Sponsor
Yeditepe University (Other)
Overall Status
Completed
CT.gov ID
NCT04045106
Collaborator
Bahçeşehir University (Other)
104
2
3
3.2
52
16.5

Study Details

Study Description

Brief Summary

the aim of the study was to investigate the immediate influence of proprioceptive neuromuscular facilitation on cervical range of motion, strength and proprioception

Condition or Disease Intervention/Treatment Phase
  • Other: Proprioceptive Neuromuscular Facilitation Patterns
  • Other: Proprioceptive Neuromuscular Facilitation stretching
  • Other: Passive range of motion
N/A

Detailed Description

the study evaluates the influence of two proprioceptive neuromuscular facilitation techniques (PNF patterns and PNF stretching) on cervical proprioception. PNF techniques are regularly used techniques among physiotherapist. also there is a lack of studies that investigated the effect of PNF on cervical proprioception

Study Design

Study Type:
Interventional
Actual Enrollment :
104 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Screening
Official Title:
The Acute Effect of Proprioceptive Neuromuscular Facilitation on Cervical Range of Motion, Strength and Proprioception
Actual Study Start Date :
Feb 20, 2019
Actual Primary Completion Date :
May 27, 2019
Actual Study Completion Date :
May 27, 2019

Arms and Interventions

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 Cervical flexion with right rotation followed by extension with left rotation. Cervical flexion with left rotation followed by extension with right rotation.

Other: Proprioceptive Neuromuscular Facilitation Patterns
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.

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.

Other: Proprioceptive Neuromuscular Facilitation stretching
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

Sham Comparator: control

Participants allocated to the control group received ineffective passive ROM.

Other: Passive range of motion
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.

Outcome Measures

Primary Outcome Measures

  1. Cervical Proprioception: Joint position accuracy method using cervical range of motion instrument. [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

Secondary Outcome Measures

  1. Range Of Motion [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.

  2. Muscle strength [1 day]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Yeditepe University Ataşehir İstanbul Turkey 34755
2 Bahcesehir University Beşiktaş Istanbul Turkey 34353

Sponsors and Collaborators

  • Yeditepe University
  • Bahçeşehir University

Investigators

  • Study Director: SULE DEMIRBASISTANBUL, Yeditepe University

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Yeditepe University
ClinicalTrials.gov Identifier:
NCT04045106
Other Study ID Numbers:
  • 10269393
First Posted:
Aug 5, 2019
Last Update Posted:
Aug 29, 2019
Last Verified:
Jul 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Yeditepe University

Study Results

No Results Posted as of Aug 29, 2019