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ProprioceptionRCTNCT04045106

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

A study testing Proprioceptive Neuromuscular Facilitation Patterns, Proprioceptive Neuromuscular Facilitation stretching and Passive range of motion in people with Proprioception and Neck, run by Yeditepe University at 2 sites in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Proprioception, Neck
What is being tested?
Proprioceptive Neuromuscular Facilitation Patterns, Proprioceptive Neuromuscular Facilitation stretching and Passive range of motion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
104 participants
Where
2 sitesTurkey (Türkiye)
Study dates
20 Feb 2019to 27 May 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Neck disability index score of 5 or less
  • Able to understand and follow instructions
  • Above 18 years old

Who cannot join

  • 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

Trial locations and contacts

2 sites in 1 country.

Turkey (Türkiye)2 sites
  • Yeditepe University

    Ataşehir, Istanbul, 34755

  • Bahcesehir University

    Beşiktaş, Istanbul, 34353

Other trials in Turkey (Türkiye)

About this study

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

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

Read the 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

Conditions
Proprioception, Neck
Being tested
Proprioceptive Neuromuscular Facilitation Patterns, Proprioceptive Neuromuscular Facilitation stretching, Passive range of motion
Keywords
Proprioception, Proprioceptive Neuromuscular Facilitation,, Cervical spine, stretching

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Proprioceptive Neuromuscular Facilitation PatternsOther

    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.

  • Proprioceptive Neuromuscular Facilitation stretchingOther

    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

  • Passive range of motionOther

    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.

Study groups in NCT04045106
Study groupRoleWhat they receive
PNF patternExperimentalPNF 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 1. Cervical flexion with right rotation followed by extension with left rotation. 2. Cervical flexion with left rotation followed by extension with right rotation.
Receives: Other: Proprioceptive Neuromuscular Facilitation Patterns
PNF stretchingExperimentalPNF stretching was done using contract-relax-antagonist contract (CRAC) technique for cervical flexors, extensors, right and left lateral flexors, right rotators and left rotators.
Receives: Other: Proprioceptive Neuromuscular Facilitation stretching
controlSham comparatorParticipants allocated to the control group received ineffective passive ROM.
Receives: Other: Passive range of motion

What is being measured

The primary outcome is the main question the study is designed to answer.

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

    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

    Measured: 1 day

Secondary outcomes (2)
  1. Range Of Motion

    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.

    Measured: 1 day

  2. Muscle strength

    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.

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Aug 2019
  2. Study start20 Feb 2019
  3. Primary completion27 May 2019
  4. Study completion27 May 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Screening
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
104 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04045106
Sponsor's protocol ID
10269393
Acronym
RCT
Status last verified
Jul 2019
First submitted
1 Aug 2019
Last updated
29 Aug 2019
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Proprioceptive Neuromuscular Facilitation Patterns, Proprioceptive Neuromuscular Facilitation stretching and Passive range of motion in people with Proprioception and Neck, run by Yeditepe University at 2 sites in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Aug 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cervical Proprioception: Joint position accuracy method using cervical range of motion instrument. (time frame: 1 day). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Aug 2019; AzTrials last refreshed its copy on 7 Nov 2026.

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