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NCT Number: NCT07058220

Effect Cervical Proprioceptive Training Cervical Proprioception Neck Pain:

Twenty-two male and female patients with neck pain participated in this study, aged from 25-40 years. They randomly distributed into 2 group: group (A, study) consisted of 11 patients received cervical proprioceptive training, while group (B, control) consisted of 11 patients received usual care. The treatment was performed 3 times per week for 1 month. The cervical proprioception (flexion, extension, right and left rotations) was assessed by Revel laser method as active joint angular reproduction [absolute error].

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Key information

Age range

25 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Twenty-two male and female patients referred from orthopedist. Patients were selected in the study if they had non-specific neck pain, aged from 25-40 years. Patients were excluded if they had positive spurling test.

All patients were randomly distributed into two groups. Group (A) or study group consisted of 11 patients received cervical proprioceptive training, while group (B) or control group consisted of 11 patients received standard care. The treatment was performed 3 times per week for 1 month. The cervical proprioception [active joint angular reproduction, absolute error] assessed by revel laser method.

Laser pointer" was used for assessing cervical proprioception. It had good reliability (r=0.68) and validity (r=0.95). The patient sat with back supported and head free to move. The target paper was fixed on the wall about 90 cm from the seat and at a distance from the ground adjusted with the height of the patient. A "laser pointer" was strapped on the highest point of the head of the patient. The patient was instructed to move the head to the tested direction (flexion and extension, and right and left rotation), then fix the laser beam at the paper center for 10 seconds while opening the eyes. The reached point in each direction was marked. Then the distance between the paper center and the reached point was measured using a tape measurement

Treatment procedures:

Cervical proprioceptive training (CPT): patients of group A received CPT through use of a laser pointer in a similar way to the testing. From sitting position, patients were asked to flex, extend and rotate their head and then return to the neutral position . This training was commenced with open eyes. Each direction was repeated 8 times for two sets, 30 seconds rest between sets. Progression of exercise was achieved by closing eyes, and altering the duration (trace shapes for 5 minutes and progress by increasing 2-3 minutes weekly as tolerated), repetitions (2-3 repetitions weekly), sets (1 set weekly) and the degree of difficulty of the task (different shapes and positions as standing and walking) .

Standard care: Patients of control group were allowed to stay active, avoid poor cervical ergonomics (poor sleeping habits, improper use of mobile/telephone),hot/cold packs, some range of motion exercises, and local medicines as prescribed by their general practitioner.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • they had non-specific neck pain

Exclusion criteria

  • they had positive spurling test.

Treatment and study plan

Cervical proprioceptive training

Other

Study group will receive proprioceptive training through use of a laser pointer in a similar way to the testing. From sitting position, patients were asked to flex, extend and rotate their head and then return to the neutral position . This training was commenced with open eyes. Each direction was repeated 8 times for two sets, 30 seconds rest between sets. Progression of exercise was achieved by closing eyes, and altering the duration (trace shapes for 5 minutes and progress by increasing 2-3 minutes weekly as tolerated), repetitions (2-3 repetitions weekly), sets (1 set weekly) and the degree of difficulty of the task (different shapes and positions as standing and walking)

ADVICES

Other

Patients of control group were allowed to stay active, avoid poor cervical ergonomics (poor sleeping habits, improper use of mobile/telephone),hot/cold packs, some range of motion exercises, and local medicines as prescribed by their general practitioner.

Primary outcomes

  1. Cervical joint position error error

    Time frame: 1 month

Study contacts

Contact information is provided by the study sponsor or research team.

Fatma Eldesoky Ramdan, Phd

CONTACT

[email protected]

0201157564905

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Physical Therapist at 23 July Hospital Marg Egypt

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jul 10, 2025
Registry last updated
Jul 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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