Actively Recruiting

Phase Not Applicable
Age: 25Years - 45Years
All Genders
ID07058220

Effect of Cervical Proprioceptive Training on Cervical Proprioception and Neck Pain

Led by Cairo University · Updated on 2025-07-10

25

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research involves men and women aged 25 to 40 years who experience non-specific neck pain. The study evaluates the effects of cervical proprioceptive training on cervical proprioception, specifically measuring joint position error using the Revel laser method. Twenty-two patients were randomly assigned to either a study group or a control group to compare different treatments for neck pain. The study group receives cervical proprioceptive training using a laser pointer. This training involves head movements including flexion, extension, and rotation while aiming a laser at a target, initially with eyes open and progressing to closed eyes and increased difficulty over time. The training occurs three times per week for one month. The control group receives standard care, including advice to stay active, avoid poor neck posture, use hot or cold packs, perform some range of motion exercises, and use local medicines prescribed by their doctor. Participants attend treatment sessions three times weekly over one month. Cervical proprioception is assessed with the Revel laser method, which measures how accurately patients can reproduce head positions. Researchers track the primary outcome of cervical joint position error after one month. The study uses double blinding and randomization to compare outcomes between the two groups, with the overall aim to understand how proprioceptive training may affect neck pain and joint position control.

CONDITIONS

Brief Title

Effect Cervical Proprioceptive Training Cervical Proprioception Neck Pain:

Who Can Participate

Age: 25Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 25 to 45 years
  • Have non-specific neck pain
  • Male or female
Not Eligible

You will not qualify if you...

  • Positive Spurling test

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 1 month

Participants receive cervical proprioceptive training or standard care to improve neck pain and cervical proprioception.

3 visits per week for 1 month

Trial Site Locations

Total: 1 location

1

Cairo y

Giza, Egypt, 11432

Actively Recruiting

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Research Team

F

Fatma Eldesoky Ramdan, Phd

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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