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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06040047
Other study ID # 012/002739
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 1, 2023
Est. completion date December 30, 2023

Study information

Verified date September 2023
Source Cairo University
Contact ElMelhat, PhD
Phone 01112595022
Email ahmedelmelhat@pt.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this predictive interventional study is todetrmine clinical predictors for success with combined proprioceptive neuromusclualr faciitaion (PNF) and passive mobilization ain patients with cervical radiculopathy (CR).


Description:

This study will answer the question, what are the factors affecting success with PNF and mobilization for patients with CR? No control group. The goal of this new study is to see the effect of age, duration of symptoms, forward posture angle and neck disability index response to passive mobilization combined with the PNF technique


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 30, 2023
Est. primary completion date December 1, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 60 Years
Eligibility Inclusion Criteria: - Participants with cervical radiculopathy. - Age ranges between 40 and 60 years old. - Minimum score (3 out of 10-point) on a visual analog scale (VAS) - Orthopedic clinical confirmation reveals a history of neck pain. Exclusion Criteria: - Whiplash injury. - Previous Cervical surgery. - Pain less than three months. - Mechanical and non-specific neck pain. - Pregnancy. - Bilateral arm pain. - Inflammatory arthritides. - Osteoporosis. - Symptoms of vertebrobasilar insufficiency.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Proprioceptive neuromuscular facilitation
Contract relax technique for each neck motion for three repetitions.
Passive mobilization
To restore normal joint play, postero-anterior passive joint mobilization of cervical spine segments and cervicothoracic junction in limited motion will be applied.

Locations

Country Name City State
Egypt ME Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cervical pain Score on numeric pain rating scale (points) 6 weeks
Primary Cervical disability Disability will be measured with Northwick Park neck pain Questionnaire. 6 weeks
Secondary Cervical proprioception Cervical joint position error will be measured with laser pointer. 6 weeks
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