Cervical Proprioception and Shoulder Impingement Treatment

NCT ID: NCT05963789

Last Updated: 2023-07-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-08-01

Study Completion Date

2023-10-31

Brief Summary

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The aim of this study will be to investigate the role of cervical proprioceptive training on shoulder proprioception, pain, and disability in shoulder impingement syndrome patients

Detailed Description

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Study design: This study will be randomized controlled trial 1. Participants: fifty males and females patients with functional shoulder impingement, aged from 25-40 years with BMI \<32kg/m2. Sample size calculation: The sample size is 50 patients in the 2 experimental groups based on power analysis done calculating effect size from outcomes of previous study (effect size d of 0.82 for shoulder proprioception) . Power analysis was done using G\*power software. Power set to (0.8), significance (0.05). Procedture: First, eligible patients will have the purpose of the study and the procedures fully explained. Then, patients will be asked to participate in the study. If they accepted, an informed consent form will be signed and randomly assigned in one of two groups. Afterwards Prior to starting of the study each patient will sign informed consent Patients will be assigned to two groups randomly (by closed envelope method). All subjects will be evaluated for their shoulder pain, disability level, and proprioception. All patients will be tested before and after the treatment program (12 treatment sessions, 3 sessions per week for 4 weeks) Conventional Physical therapy: a. Cross-body stretch b. Sleeper stretch. c. Prone extension with an externally rotated (thumb out) position d. Prone horizontal abduction e. PNF D2 flexion For intervention group it will take Cervical proprioceptive training Retraining joint position sense will be done with a laser pointer. The laser pointer will fixed on the highest point of the subject head with a band. In this exercise, patients sit upright on a chair and kept their head at the neutral position while setting the laser light at the point on the wall in front of them. From this position, patients will be asked to flex, extend and rotate their head and then return to the neutral position. This training commenced with open eyes and then progress with closed eyes, tracing a pattern and standing position . Temporary reproduction of dizziness is acceptable however exacerbation of neck pain or headache is not acceptable. If this occurs the exercises should be modified by decreasing the number of repetitions or altering the patient position to a more supported position. Progression of exercise set can be achieved by altering the duration, repetitions and the degree of difficulty of the task. Exercises can also be progressed by performing activities such as an eye task or cervical JPS practice while sitting on an unstable surface or while standing with the feet in an unstable base of support for example, heel toe stance, or while walking .

Conditions

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Shoulder Impingement Shoulder Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Group A or cervical proprioception group CPG

Patients will receive traditional exercises for shoulder impingement plus cervical proprioception exercises using laser pointer

Group Type EXPERIMENTAL

Cervical proprioceptive training

Intervention Type OTHER

Cervical proprioceptive training: The laser pointer will fixed on the highest point of the subject head with a band, patients sit upright on a chair and kept their head at the neutral position, while setting the laser light at the point on the wall in front of them. From this position, patients will be asked to flex, extend and rotate their head and then return to the neutral position. This training commenced with open eyes and then progress with closed eyes, tracing a pattern and standing position.

Group B or control group CG

Patients will receive traditional exercises for shoulder impingement (stretching, strengthening, stabilization)

Group Type ACTIVE_COMPARATOR

Traditional exercises

Intervention Type OTHER

Stretching posterior shoulder capsule Strengthening scapular muscles Shoulder stabilization PNF

Interventions

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Cervical proprioceptive training

Cervical proprioceptive training: The laser pointer will fixed on the highest point of the subject head with a band, patients sit upright on a chair and kept their head at the neutral position, while setting the laser light at the point on the wall in front of them. From this position, patients will be asked to flex, extend and rotate their head and then return to the neutral position. This training commenced with open eyes and then progress with closed eyes, tracing a pattern and standing position.

Intervention Type OTHER

Traditional exercises

Stretching posterior shoulder capsule Strengthening scapular muscles Shoulder stabilization PNF

Intervention Type OTHER

Other Intervention Names

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Traditional exercises

Eligibility Criteria

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Inclusion Criteria

* Shoulder impingement syndrome (defined as patients with at least 3 out of the following 6 criteria; Positive "Neer's sign", Positive "Hawkins' sign", Pain with active shoulder elevation in the scapular plane, Pain in the C5-C6 dermatome, Pain with palpation of the rotator cuff tendons, and Pain with resisted isometric abduction.
* Patients with positive apprehension sign for anterior instability.
* Age 25-40years. 4-BMI\<32 kg/m2.

Exclusion Criteria

* Shoulder osteoarthritis

* Shoulder trauma
* Shoulder infection
* Intra-articular corticosteroid or hyaluronic acid injection within the last 3 months.
* Previous surgery of the affected shoulder. - Symptomatic cervical pathology.
Minimum Eligible Age

25 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Fatma eldesoky

Physiotherapist at 23rd of July hospital, PhD candidate physiotherapy, Cairo university

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Abdel Majeed

Role: PRINCIPAL_INVESTIGATOR

Professor at orthopedic department, faculty of physical therapy, Cairo University

Locations

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Fatma eldesoky Ramadan

Cairo, Cairo Governorate, Egypt

Site Status RECRUITING

Countries

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Egypt

Central Contacts

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Salwa F Abdel Majeed

Role: CONTACT

01008565476

Facility Contacts

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Fatma Eldesoki, Doctoral

Role: primary

01157564905

Fatma Eldesoky, Doctoral

Role: backup

01157564905

Other Identifiers

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P.T.REC/012/004185

Identifier Type: -

Identifier Source: org_study_id

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