Shoulder Impingement SyndromeNCT05318209
Effect of Closed-chain Shoulder Girdle Scapular Depression Exercise on Shoulder Impingement Syndrome
A study testing Exercise in people with Shoulder Impingement Syndrome, run by Nasr Awad Abdelkader Othman at 1 site in Egypt.
Trial summary
forty patients will be assigned randomly into 2 equal groups Study group (n=23) will receive "closed-chain shoulder girdle scapular depression exercise" in addition to Stretching for posterior capsule \& pectoralis minor, Eccentric exercise for external rotators and Strength exercises for serrates anterior and low… Read more about this study
- Who is it for?
- Ages 25 to 45 years
- Conditions the study is for
- Shoulder Impingement Syndrome
- What is being tested?
- Exercise
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 46 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Feb 2024to 1 Dec 2024
- 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 25 to 45 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Patients aged from 25 to 45 years old.
- Patients with shoulder impingement stage I \&II as judged by criteria of neer classification.
- Patients diagnosed by orthopedic surgeon with shoulder impingement, the diagnosis will be confirmed by positive Neer and Hawkins tests.
Who cannot join
- History of cardiac diseases or dyspnea on exertion
- Patients with cervical radiculopathy.
- Patients with shoulder instability.
- Patients with frozen shoulder.
- Acute shoulder trauma.
Trial locations and contacts
1 site in 1 country.
Egypt1 site, 1 recruiting
- Recruiting
Kafr Elshiekh Hospital
Kafr ash Shaykh
Atef A. Nadier, PhD, 00201003867064, atef.neder@pua.edu.eg
About this study
Official title: Comparison Between Closed-chain Shoulder Girdle Scapular Depression Exercise and Shoulder Girdle Depression Against Manual Resistance on Patients With Shoulder Impingement Syndrome
forty patients will be assigned randomly into 2 equal groups Study group (n=23) will receive "closed-chain shoulder girdle scapular depression exercise" in addition to Stretching for posterior capsule \& pectoralis minor, Eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound Control group B (n=23) will receive "shoulder girdle depression against manual resistance exercise" in addition to stretching for posterior capsule \& pectoralis minor, eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound .
The exercise program will consist of 3 sessions / week for 5 weeks
Read the detailed description
BACKGROUND:
Patients with shoulder impingment syndrome report disability, especially during overhead movements, which may hinder activities of daily living .
Muscular strengthening training influences the resting position and scapular movement pattern of subjects with shoulder impingement syndrome and improve function of the affected shoulder.
Therefore, the focus of treatment for the syndrome is on performing exercises, including stretching, strengthening, and neuromuscular control exercises.
Although multiple types of exercise, such as scapular stability exercises, strengthening of the rotator cuff through range, and flexibility exercises for the anterior and posterior shoulder exercise is effective in the management of patients with shoulder impingement syndrome, there is not enough evidence to say whether one mode of exercise is superior to another.
RESEARCH QUESTION:
Are there any difference between closed-chain shoulder girdle scapular depression exercise and shoulder girdle depression against manual resistance exercise on patients with shoulder impingement syndrome
METHODS:
forty patients will be assigned randomly into 2 equal groups Study group (n=23) will receive "closed-chain shoulder girdle scapular depression exercise" in addition to Stretching for posterior capsule \& pectoralis minor, Eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound Control group B (n=23) will receive "shoulder girdle depression against manual resistance exercise" in addition to stretching for posterior capsule \& pectoralis minor, eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound .
The exercise program will consist of 3 sessions / week for 5 weeks
- Conditions
- Shoulder Impingement Syndrome
- Being tested
- Exercise
- Medical subject headings
- Shoulder Impingement Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ExerciseOther
Closed-chain Shoulder Girdle Scapular Depression Exercise
| Study group | Role | What they receive |
|---|---|---|
| Study grou[p | Experimental | Closed-chain shoulder girdle scapular depression exercise Receives: Other: Exercise |
| control group | Active comparator | Shoulder girdle depression against manual resistance exercise Receives: Other: Exercise |
What is being measured
The primary outcome is the main question the study is designed to answer.
Pain will be measured by visual analogue scale
10cm visual analogue scale (0= no pain, and 10= maximum pain) will be used to determine overall shoulder pain
Measured: 10 minutes
Secondary outcomes (2)
Range of motion (flexion and abduction) will be measured by Electronic goniometer
Electronic Goniometer will be used to measure shoulder range of motion (Flexion and abduction)
Measured: 20 minutes
Function
shoulder function will be measured by western Ontario Rotator Cuff Questionnaire (WORC).
Measured: 30 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Apr 2022
- Study start1 Feb 2024 (estimated)
- Primary completion1 Mar 2024 (estimated)
- Study completion1 Dec 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Shoulder Impingement SyndromeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 46 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Nasr Awad Abdelkader Othman
- Sponsor type
- University, hospital or other
- Collaborators
- Pharos University in Alexandria, Horus University
- Responsible party
- Sponsor-investigator, Nasr Awad Abdelkader Othman, Cairo University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05318209
- Sponsor's protocol ID
- P.T.REC/012/003377
- Status last verified
- Feb 2024
- First submitted
- 21 Mar 2022
- Last updated
- 8 Feb 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 8 Feb 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison Between Closed-chain Shoulder Girdle Scapular Depression Exercise and Shoulder Girdle Depression Against Manual Resistance on Patients With Shoulder Impingement Syndrome
- ClinicalTrials.gov ID
- NCT05318209
- Acronym / sponsor ID
- P.T.REC/012/003377
- Conditions
- Shoulder Impingement Syndrome
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 46 participants (estimated)
- Lead sponsor
- Nasr Awad Abdelkader OthmanUniversity, hospital or other
- Collaborators
- Pharos University in Alexandria, Horus University
- Study start
- 1 Feb 2024 (estimated)
- Primary completion
- 1 Mar 2024 (estimated)
- Study completion
- 1 Dec 2024 (estimated)
- First posted
- 8 Apr 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
forty patients will be assigned randomly into 2 equal groups Study group (n=23) will receive "closed-chain shoulder girdle scapular depression exercise" in addition to Stretching for posterior capsule \& pectoralis minor, Eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound Control group B (n=23) will receive "shoulder girdle depression against manual resistance exercise" in addition to stretching for posterior capsule \& pectoralis minor, eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound .
The exercise program will consist of 3 sessions / week for 5 weeks
Detailed description
BACKGROUND:
Patients with shoulder impingment syndrome report disability, especially during overhead movements, which may hinder activities of daily living .
Muscular strengthening training influences the resting position and scapular movement pattern of subjects with shoulder impingement syndrome and improve function of the affected shoulder.
Therefore, the focus of treatment for the syndrome is on performing exercises, including stretching, strengthening, and neuromuscular control exercises.
Although multiple types of exercise, such as scapular stability exercises, strengthening of the rotator cuff through range, and flexibility exercises for the anterior and posterior shoulder exercise is effective in the management of patients with shoulder impingement syndrome, there is not enough evidence to say whether one mode of exercise is superior to another.
RESEARCH QUESTION:
Are there any difference between closed-chain shoulder girdle scapular depression exercise and shoulder girdle depression against manual resistance exercise on patients with shoulder impingement syndrome
METHODS:
forty patients will be assigned randomly into 2 equal groups Study group (n=23) will receive "closed-chain shoulder girdle scapular depression exercise" in addition to Stretching for posterior capsule \& pectoralis minor, Eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound Control group B (n=23) will receive "shoulder girdle depression against manual resistance exercise" in addition to stretching for posterior capsule \& pectoralis minor, eccentric exercise for external rotators and Strength exercises for serrates anterior and low intensity ultrasound .
The exercise program will consist of 3 sessions / week for 5 weeks
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Study grou[p | Experimental | Other: ExerciseClosed-chain shoulder girdle scapular depression exercise |
| control group | Active comparator | Other: ExerciseShoulder girdle depression against manual resistance exercise |
Who may qualify
- Ages
- 25 to 45 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- Patients aged from 25 to 45 years old.
- Patients with shoulder impingement stage I \&II as judged by criteria of neer classification.
- Patients diagnosed by orthopedic surgeon with shoulder impingement, the diagnosis will be confirmed by positive Neer and Hawkins tests.
Key exclusion criteria (5 listed)
- History of cardiac diseases or dyspnea on exertion
- Patients with cervical radiculopathy.
- Patients with shoulder instability.
- Patients with frozen shoulder.
- Acute shoulder trauma.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ExerciseClosed-chain Shoulder Girdle Scapular Depression Exercise | Other | Study grou[p, control group |
Primary outcome
Pain will be measured by visual analogue scale
Time frame: 10 minutes
10cm visual analogue scale (0= no pain, and 10= maximum pain) will be used to determine overall shoulder pain
2 secondary outcomes
Range of motion (flexion and abduction) will be measured by Electronic goniometer
Time frame: 20 minutes
Function
Time frame: 30 minutes
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Feb 2024.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Exercise in people with Shoulder Impingement Syndrome, run by Nasr Awad Abdelkader Othman at 1 site in Egypt.
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 5 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: status not confirmed, as of the sponsor's last update on 8 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. 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. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Nasr A. Abdelkader, PhD (00201025771117, dr.nasrawad@cu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Pain will be measured by visual analogue scale (time frame: 10 minutes). 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 8 Feb 2024.