Chronic Shoulder PainNCT07065045
Psychometric Properties Of Translated Arabic Version Of The Fremantle Shoulder Awareness Questionnaire In Patients With Chronic Shoulder Pain
An observational study of Chronic Shoulder Pain, run by Cairo University.
Trial summary
Test the psychometric properties of translated arabic version of the Fremantle shoulder awareness questionnaire in patients with chronic shoulder pain Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Shoulder Pain
- How many people
- 200 participants
- Where
- No sites listed yet
- Study dates
- 1 Sep 2025to 15 Feb 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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 18 years and older
- All sexes
- Adult, Older adult
Study population: Patients with chronic shoulder pain will be aged 18 or more years old . Shoulder pain lasting for more than three months who, after clinical evaluation, will be positive in at least three of the following six clinical tests: (1) Hawkins impingement sign; (2) Neer's impingement sign; (3) painful arc sign; (4) Jobe's test; (5) Whipple's test; (6) shoulder pain elicited by resistance testing during shoulder abduction or external rotation. Being conscious and oriented. Able to read and write in Arabic.
Who may be able to join
- Patients with chronic shoulder pain was aged 18 or more years old .
- Shoulder pain lasting for more than three months which, after clinical evaluation, was positive in at least three of the following six clinical tests: (1) Hawkins impingement sign; (2) Neer's impingement sign; (3) painful arc sign; (4) Jobe's test; (5) Whipple's test; (6) shoulder pain elicited by resistance testing during shoulder abduction or external rotation.
- Being conscious and oriented.
- Able to read and write in Arabic.
Who cannot join
- History of shoulder surgery or planned shoulder surgery.
- History of fracture, dislocation, or degenerative disease of the shoulder joint.
- Active shoulder range of motion <90 degrees of flexion or abduction or <0 degrees of external rotation.
- Cervical radiculopathy or examination that caused shoulder pain/reduced range of motion after repetitive neck movements.
- Other serious orthopedic problems.
About this study
Test the psychometric properties of translated arabic version of the Fremantle shoulder awareness questionnaire in patients with chronic shoulder pain
- Conditions
- Chronic Shoulder Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Patient with chronic shoulder pain | Patients with chronic shoulder pain will be aged 18 or more years old . Shoulder pain lasting for more than three months who, after clinical evaluation, will be positive in at least three of the following six clinical tests: (1) Hawkins impingement sign; (2) Neer's impingement sign; (3) painful arc sign; (4) Jobe's test; (5) Whipple's test; (6) shoulder pain elicited by resistance testing during shoulder abduction or external rotation. Being conscious and oriented. Able to read and write in Arabic. |
What is being measured
The primary outcome is the main question the study is designed to answer.
validity
questionnaires will be given to chronic painful shoulder patients. Face validity and content validity will be tested by asking physiotherapists who are experienced for > five years if arabic version of the fremantle shoulder awareness questionnaire is easy to use and its contents relevant to the title. construct validity will be tested by applying questionnaires to patients with chronic shoulder pain as gold standard: cross-culturally adapted arabic version of the fremantle shoulder awareness questionnaire(score 0-36, Higher scores indicate greater levels of disturbed bodily self-awareness),Pain Visual Analogue Scale(score 0-100, higher score indicates greater pain intensity), the Quick Disabilities of the Arm, Shoulder and Hand questionnaire(score 0-100 and higher score indicates greater disability),the Shoulder Pain and Disability Index (score 0-10, higher score indicates pain and disability) and the Pain Catastrophizing Scale(score 0-52, higher score indicates high pain perception)
Measured: One week
Reliability
The participants will fill in the Fremantle shoulder awareness questionnaire Arabic version again after 5-7 days without any intervening physical therapy session between those two occasions and at the same time of day to assess the test-retest reliability of the scale. Its overall score ranges from 0-36. Higher scores are associated with greater levels of disturbed bodily self-awareness
Measured: one week
feasibility (the time needed to fill out the translated Arabic version of the fremantle shoulder awareness questionnaire.)
The researcher will calculate the time needed to fill out the translated Arabic version of the fremantle shoulder awareness questionnaire.
Measured: one week
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Jul 2025
- Study start1 Sep 2025 (estimated)
- Primary completion30 Jan 2026 (estimated)
- Study completion15 Feb 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Shoulder PainStudies of the same condition, open and under way.
- More trials run by Cairo UniversityThe sponsor's other registered studies.
- 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
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Cairo University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, salma khamis mohamed El-gazzar, Cairo University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07065045
- Sponsor's protocol ID
- P.T.REC/012/005859
- Status last verified
- Jul 2025
- First submitted
- 10 Jun 2025
- Last updated
- 15 Jul 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 15 Jul 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Psychometric Properties Of Translated Arabic Version Of The Fremantle Shoulder Awareness Questionnaire In Patients With Chronic Shoulder Pain
- ClinicalTrials.gov ID
- NCT07065045
- Acronym / sponsor ID
- P.T.REC/012/005859
- Conditions
- Chronic Shoulder Pain
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Cairo UniversityUniversity, hospital or other
- Study start
- 1 Sep 2025 (estimated)
- Primary completion
- 30 Jan 2026 (estimated)
- Study completion
- 15 Feb 2026 (estimated)
- First posted
- 15 Jul 2025 (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.
Test the psychometric properties of translated arabic version of the Fremantle shoulder awareness questionnaire in patients with chronic shoulder pain
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patient with chronic shoulder pain | – | –Patients with chronic shoulder pain will be aged 18 or more years old . Shoulder pain lasting for more than three months who, after clinical evaluation, will be positive in at least three of the following six clinical tests: (1) Hawkins impingement sign; (2) Neer's impingement sign; (3) painful arc sign; (4) Jobe's test; (5) Whipple's test; (6) shoulder pain elicited by resistance testing during shoulder abduction or external rotation. Being conscious and oriented. Able to read and write in Arabic. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Patients with chronic shoulder pain will be aged 18 or more years old . Shoulder pain lasting for more than three months who, after clinical evaluation, will be positive in at least three of the following six clinical tests: (1) Hawkins impingement sign; (2) Neer's impingement sign; (3) painful arc sign; (4) Jobe's test; (5) Whipple's test; (6) shoulder pain elicited by resistance testing during shoulder abduction or external rotation. Being conscious and oriented. Able to read and write in Arabic.
Key inclusion criteria (4 listed)
- Patients with chronic shoulder pain was aged 18 or more years old .
- Shoulder pain lasting for more than three months which, after clinical evaluation, was positive in at least three of the following six clinical tests: (1) Hawkins impingement sign; (2) Neer's impingement sign; (3) painful arc sign; (4) Jobe's test; (5) Whipple's test; (6) shoulder pain elicited by resistance testing during shoulder abduction or external rotation.
- Being conscious and oriented.
- Able to read and write in Arabic.
Key exclusion criteria (5 listed)
- History of shoulder surgery or planned shoulder surgery.
- History of fracture, dislocation, or degenerative disease of the shoulder joint.
- Active shoulder range of motion <90 degrees of flexion or abduction or <0 degrees of external rotation.
- Cervical radiculopathy or examination that caused shoulder pain/reduced range of motion after repetitive neck movements.
- Other serious orthopedic problems.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
validity
Time frame: One week
questionnaires will be given to chronic painful shoulder patients. Face validity and content validity will be tested by asking physiotherapists who are experienced for > five years if arabic version of the fremantle shoulder awareness questionnaire is easy to use and its contents relevant to the title. construct validity will be tested by applying questionnaires to patients with chronic shoulder pain as gold standard: cross-culturally adapted arabic version of the fremantle shoulder awareness questionnaire(score 0-36, Higher scores indicate greater levels of disturbed bodily self-awareness),Pain Visual Analogue Scale(score 0-100, higher score indicates greater pain intensity), the Quick Disabilities of the Arm, Shoulder and Hand questionnaire(score 0-100 and higher score indicates greater disability),the Shoulder Pain and Disability Index (score 0-10, higher score indicates pain and disability) and the Pain Catastrophizing Scale(score 0-52, higher score indicates high pain perception)
Reliability
Time frame: one week
The participants will fill in the Fremantle shoulder awareness questionnaire Arabic version again after 5-7 days without any intervening physical therapy session between those two occasions and at the same time of day to assess the test-retest reliability of the scale. Its overall score ranges from 0-36. Higher scores are associated with greater levels of disturbed bodily self-awareness
feasibility (the time needed to fill out the translated Arabic version of the fremantle shoulder awareness questionnaire.)
Time frame: one week
The researcher will calculate the time needed to fill out the translated Arabic version of the fremantle shoulder awareness questionnaire.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Jul 2025.
Related trials for Chronic Shoulder Pain
RecruitingObservational study
Nociplastic Pain in Patients Diagnosed With Subacromial Pain Syndrome (SAPS)
Subacromial Pain Syndrome, Rotator Cuff Related Shoulder Pain
RecruitingObservational study
Pain Phenotype and Response to Corticosteroid Injection in Patients With Subacromial Pain Syndrome (SAPS)
Subacromial Pain Syndrome, Rotator Cuff Related Shoulder Pain
Recruiting
Effects of Rotator Cuff Drills Versus Progressive Resistance Exercises on Chronic Rotator Cuff Tendinopathy
Rotator Cuff Tendinosis
RecruitingObservational study
Prospective Case Series Evaluating 6-Month and 12-Month Outcomes After Cryoneurolysis for Chronic Pain
Chronic Pain, PERIPHERAL NEUROPATHY
Active, not recruiting
Precision Medicine for Nociception, Sngception and Proprioception.
Rehabilitation, Pain, Shoulder
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.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Chronic Shoulder Pain, run by Cairo University.
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 4 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: opening soon, as of the sponsor's last update on 15 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.
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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
validity (time frame: One week). The study lists 3 primary outcomes in all. 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 15 Jul 2025; AzTrials last refreshed its copy on 8 Nov 2026.