Subacromial Impingement SyndromeNCT06107985
To Develop and Validate a Structured Exercise Protocol and Its Efficacy in Sub Acromial Impingement Patients
A study testing Structured exercise program and Conventional Exercise Program in people with Subacromial Impingement Syndrome, run by Hamad Medical Corporation.
Trial summary
Shoulder impingement syndrome (SIS) is responsible for 44% to 60% of medical consultations related to shoulder pain with an approximate prevalence of 70-200 per 1000 adults, which implies a remarkable use of health care resources. Read more about this study
- Who is it for?
- Ages 18 to 60 years
- Conditions the study is for
- Subacromial Impingement Syndrome
- What is being tested?
- Structured exercise program and Conventional Exercise Program
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 90 participants
- Where
- No sites listed yet
- Study dates
- Dec 2023to Feb 2025
- 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 18 to 60 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Age group between 18-60 years
- Symptoms for more than three weeks
- Main complaints in the gleno humeral joint region or the proximal arm
- Presence of one of the following signs indicating SAIS: Neer impingement test, Hawkins-Kennedy impingement test, painful arc with active abduction or flexion. Pain with one of the following resistance tests: external rotation, internal rotation, abduction
Who cannot join
- Severe pain; pain is > 7/10 on NRS (0 = no pain)
- Shoulder surgery on affected shoulder
- Traumatic shoulder dislocation/ fracture within the past 3 months
- Previous rehabilitation for this episode of shoulder pain
- Reproduction of shoulder pain with active or passive cervical motion
- Systemic inflammatory joint disease
Show all 11Show fewer
- Global loss of passive shoulder ROM, indicative of adhesive capsulitis
- Full-thickness rotator cuff tear
- Incompetent adults
- Subjects unable to consent
- Patients who are unfit to undergo the suggested exercises as per the protocol
Trial locations and contacts
No sites are listed yet.
About this study
Official title: To Develop and Validate a Structured Exercise Protocol and to Assess Its Effectiveness in Patients With Sub Acromial Impingement Syndrome
Shoulder impingement syndrome (SIS) is responsible for 44% to 60% of medical consultations related to shoulder pain with an approximate prevalence of 70-200 per 1000 adults, which implies a remarkable use of health care resources. The cost for society is high and patients with shoulder disorders account for 20% of all disability due to musculoskeletal disorder. The underlying mechanisms are thought to include inflammation, degeneration of the tendons or bursa, dysfunctional scapulothoracic and glenohumeral mechanics, debilitated scapular musculature, joint capsule irregularities, postural abnormalities of the neck and shoulder, and morphological abnormalities of the relevant skeletal elements. There is a need for well-designed structured exercise program in detail considering content, dosage and progression to guide treatment for patients with sub acromial pain.
The purpose of this study is to develop and validate a structured exercise protocol and to assess its effectiveness in patients with sub-acromial impingement syndrome. Through the extensive literature review, the exercise program would be proposed. In Phase 1, We will develop and validate a structured exercise programs for sub acromial impingement syndrome using an expert consensus Delphi-based survey technique. In phase 2, a randomized controlled trial will be conducted. Group A (Experimental Group) will receive newly structured exercises for twelve weeks and Group B (control group) will receive conventional exercise program for 12 weeks. Evaluation of the participant will be done at the baseline using Constant Murley Score, shoulder pain and disability Index (SPADI). Shoulder range of motion, shoulder muscles extensibility will be assessed and scapulothoracic ratio will be calculated and documented. T-FAST test will be conducted to score the patients functional performance.
Assessment will be done at baseline, 3, 6, 9, and 12 weeks in both the groups. At the end of the study the data will be collected, coded and tabulated using descriptive and inferential statistics.
Read the detailed description
Shoulder pain is very common with an annual population prevalence of up to 46.7%, and a lifetime prevalence of up to 67%.1 In primary care, shoulder pain is the third most common musculoskeletal presentation. 1, 2 Shoulder pain may have an unfavourable outcome, with only about 50% of all new episodes of shoulder complaints presenting in physiotherapy practice showing a complete recovery within 6 months. Symptoms may be disabling in terms of the patient's ability to carry out daily activities at home and at the workplace. The most frequent shoulder diagnosis is subacromial pain syndrome, affecting about half of all shoulder patients, both in general practice and in secondary care. Shoulder impingement syndrome (SIS) is responsible for 44% to 60% of medical consultations related to shoulder pain implies a remarkable use of health care resources. The cost for society is high and patients with shoulder disorders account for 20% of all disability due to musculoskeletal disorder. The diagnosis of SIS is therefore mainly based on functional aspects and on an affected anatomical structure and requires a thorough history and clinical examination, including aspects such as activity and participation restrictions, aggravating and easing factors, or the "patients' perspective on the situation". Physiotherapy assessment has a very significant role to find out the structural and functional impairments and accordingly set the goals of management. Diagnosing the cause and identifying the source or affected structure is of utmost importance in Physiotherapy management. Apart from focusing only on structures, physiotherapy assessment emphasizes on movement dysfunctions and biomechanical derangements commonly seen in patients with impingement. Correction of the biomechanical faults would off load the sub acromial space and reduce the pain. The technique used to correct the biomechanics is called "load modification or Shoulder symptom modification process" and involves techniques: Alterations to thoracic kyphosis, Scapular positioning techniques, Humeral head positioning procedures and pain and symptom neuromodulation procedure. Current evidence for the physiotherapeutic treatment of SIS, summarized in systematic reviews through the last years, supports the specific and structured exercise program. Furthermore, these studies used either different types of exercises in their groups as a basic treatment, or applied a pre-defined set of manual techniques to all patients without considering the individual situation of the patient. Reasons for the selection or the combination of the exercises or the manual techniques used varied considerably between studies, were often not explained and thus remained unclear. Recent systematic review and meta-analysis conducted by Louis Pieter and Jeremy Lewis in 2020 concluded that continued research is needed to more fully understand the uncertainty around the optimal type, dose, and duration of exercise for sub-acromial shoulder pain. Thus, nearly all current systematic reviews emphasize the need for more high quality trials of physiotherapy interventions to optimize the dosimetry of exercise program. The term conventional physiotherapy is uninterpretable and inconclusive especially because there is presumption of how exactly the exercise program is formed. Many of the exercise program do not provide adequate information of what and why interventions are used. There are many varieties of exercises with different rationale and techniques. Hence, it is mandatory to have an adequate description of techniques making up the intervention and rationale for dosage is essential i.e. the number of sessions, intensity, and duration of intervention as per the TIDieR checklist (Template for Intervention description and replication). There is a need for well-designed structured exercise program in detail considering content, dosage and progression to guide treatment for patients with sub acromial pain. This demands developing a specific guidance on how exercise interventions should be reported in clinical trials depending on what structure is affected in intrinsic and extrinsic mechanisms of subacromial impingement syndrome. 4 The purpose of this study is to develop and validate a structured exercise protocol and to assess its effectiveness in patients with sub-acromial impingement syndrome. Through the extensive literature review, the exercise program would be proposed. We will develop and evaluate a structured exercise programs for sub acromial impingement syndrome using an expert consensus Delphi-based survey technique. Structured exercise program will be formed as per the guidelines of TIDieR items which will include the name of the intervention; intervention rationale for essential elements; intervention materials and details about how to access them; description of the intervention procedures; details of intervention providers; mode of delivery of intervention; location of intervention delivery and key infrastructure; details about the number, duration, intensity, and dose of intervention sessions; details of any intervention tailoring; any intervention modifications throughout the study; and details of intervention assessment, monitoring, and level achieved. This intervention will be based on shoulder kinetic control, load modification exercises and lumbopelvic stabilization with core stability exercises which is not a part of conventional exercise program for shoulder impingement syndrome patients. The study will be conducted in two phases. Phase 1 will be to develop and validate a structured exercise program and phase 2 is to evaluate efficacy of structured exercises on pain, range of motion and shoulder functions using Constant Murley score and Shoulder Pain and Disability Index (SPADI) and functional performance using timed functional arm and shoulder test. A randomized controlled trial will be conducted. Group A (Experimental Group) will receive structured exercises for twelve weeks and Group B (control group) will receive conventional exercise program for 12 weeks. Evaluation of the participant will be done at the baseline using Constant Murley Score, shoulder pain and disability Index (SPADI). Shoulder range of motion, shoulder muscles extensibility will be assessed and scapulothoracic ratio will be calculated and documented. T-FAST test will be conducted to score the patients functional performance. Assessment will be done at baseline, 3, 6, 9, and 12 weeks in both the groups. At the end of the study the data will be collected, coded and tabulated using descriptive and inferential statistics. The data will be analyzed to see the efficacy of newly developed structured exercise program versus conventional exercise program.
- Conditions
- Subacromial Impingement Syndrome
- Being tested
- Structured exercise program, Conventional Exercise Program
- Keywords
- Subacromial Impingement, exercise protocol, SPADI
- 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.
Structured exercise programOther
This intervention will be based on shoulder kinetic control, load modification exercises and lumbopelvic stabilization with core stability exercises which is not a part of conventional exercise program for shoulder impingement syndrome patients.
Conventional Exercise ProgramOther
Conventional exercise program for shoulder impingement syndrome patients
| Study group | Role | What they receive |
|---|---|---|
| Structured exercise group | Experimental | Group A (Experimental Group) will receive structured exercises protocol, will be given approximately for two days per week for twelve weeks. Receives: Other: Structured exercise program |
| Conventional Exercise group | Active comparator | Group B (control group) will receive conventional exercise program for two days per week for twelve weeks. Receives: Other: Conventional Exercise Program |
What is being measured
The primary outcome is the main question the study is designed to answer.
Constant-Murley Score
This score is a shoulder-specific assessment tool containing objective measures (range of movement and shoulder strength) and subjective measures (activity of daily living and pain). This scale assesses four aspects related to shoulder pathology; two subjective: pain and activities of daily living (ADL) and two objectives: range of motion (ROM) and strength. The subjective components can receive up to 35 points and the objective 65, resulting in a possible maximum total score of 100 points (best function). Pain and ADL are answered by the patient; ROM and strength require a physical evaluation and are answered by the physiotherapist.
Measured: Baseline, 3, 6, 9, and 12 weeks
Visual analouge Scale
The visual analogue scale (VAS; 0-10) is used to assess the patient's perceived pain intensity at rest, during arm activity and at night during the previous 24 hours at each follow-up. The visual analogue scale (VAS) uses a 10 cm line with endpoint descriptors such as 'no pain' marked at the left end of the line and 'worst pain imaginable' marked at the right end. Patients are asked to mark a point on the line that best represents their pain. The distance from 'no pain' to the patient's mark is then measured and this equals the Visual Analouge scale score.
Measured: Baseline, 3, 6, 9, and 12 weeks
The Shoulder Pain and Disability Index (SPADI)
The Shoulder Pain and Disability Index is a self-administered questionnaire that consists of two dimensions, one for pain and the other for functional activities. The pain dimension consists of five questions regarding the severity of an individual's pain. Functional activities are assessed with eight questions designed to measure the degree of difficulty an individual has with various activities of daily living that require upper-extremity use. To answer the questions, patients place a mark on a 10cm visual analogue scale for each question. Verbal anchors for the pain dimension are 'no pain at all' and 'worst pain imaginable', and those for the functional activities are 'no difficulty' and 'so difficult it required help'. The scores from both dimensions are averaged to derive a total score. The means of the two subscales are averaged to produce a total score ranging from 0 (best) to 100 (worst).
Measured: Baseline, 3, 6, 9, and 12 weeks
Timed Functional Arm and Shoulder Test
The Timed Functional Arm and Shoulder Test (TFAST)is a simple battery of physical performance tests for functional task used for shoulder assessment.
Measured: Baseline, 3, 6, 9, and 12 weeks
Secondary outcomes (1)
Scapulothoracic ratio Measurement
Scapulothoracic ratio is measured with inclinometer to quantify scapular upward rotation associated with varying amounts of humeral elevation for measurement of scapular upward rotation
Measured: Baseline, 3, 6, 9, and 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Oct 2023
- Study startDec 2023 (estimated)
- Primary completionDec 2024 (estimated)
- Study completionFeb 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (5)Papers the sponsor has linked to this study.
- Other trials for Subacromial 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
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 90 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hamad Medical Corporation
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Seth Gordhandas Sunderdas Medical College
- Responsible party
- Principal investigator, Reshma Shashank Gurav, Hamad Medical Corporation
- Investigators
- Reshma Gurav, Principal investigator, Hamad Medical Corporation
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06107985
- Sponsor's protocol ID
- MRC-01-22-428
- Other IDs
- EC-OA-94-2022
- Status last verified
- Oct 2023
- First submitted
- 1 Oct 2023
- Last updated
- 30 Oct 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Ludewig PM, Cook TM. Alterations in shoulder kinematics and associated muscle activity in people with symptoms of shoulder impingement. Phys Ther. 2000 Mar;80(3):276-91.
PubMed 10696154Shire AR, Staehr TAB, Overby JB, Bastholm Dahl M, Sandell Jacobsen J, Hoyrup Christiansen D. Specific or general exercise strategy for subacromial impingement syndrome-does it matter? A systematic literature review and meta analysis. BMC Musculoskelet Disord. 2017 Apr 17;18(1):158. doi: 10.1186/s12891-017-1518-0.
PubMed 28416022Kromer TO, de Bie RA, Bastiaenen CH. Effectiveness of individualized physiotherapy on pain and functioning compared to a standard exercise protocol in patients presenting with clinical signs of subacromial impingement syndrome. A randomized controlled trial. BMC Musculoskelet Disord. 2010 Jun 9;11:114. doi: 10.1186/1471-2474-11-114.
PubMed 20534140Pieters L, Lewis J, Kuppens K, Jochems J, Bruijstens T, Joossens L, Struyf F. An Update of Systematic Reviews Examining the Effectiveness of Conservative Physical Therapy Interventions for Subacromial Shoulder Pain. J Orthop Sports Phys Ther. 2020 Mar;50(3):131-141. doi: 10.2519/jospt.2020.8498. Epub 2019 Nov 15.
PubMed 31726927Worsley P, Warner M, Mottram S, Gadola S, Veeger HE, Hermens H, Morrissey D, Little P, Cooper C, Carr A, Stokes M. Motor control retraining exercises for shoulder impingement: effects on function, muscle activation, and biomechanics in young adults. J Shoulder Elbow Surg. 2013 Apr;22(4):e11-9. doi: 10.1016/j.jse.2012.06.010. Epub 2012 Sep 1.
PubMed 22947240
Study at a glance
From the registry record, last updated by the sponsor on 30 Oct 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- To Develop and Validate a Structured Exercise Protocol and to Assess Its Effectiveness in Patients With Sub Acromial Impingement Syndrome
- ClinicalTrials.gov ID
- NCT06107985
- Acronym / sponsor ID
- MRC-01-22-428
- Conditions
- Subacromial Impingement Syndrome
- Keywords
- Subacromial Impingement, exercise protocol, SPADI
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 90 participants (estimated)
- Lead sponsor
- Hamad Medical CorporationIndustry (pharma, biotech, devices)
- Collaborators
- Seth Gordhandas Sunderdas Medical College
- Study start
- Dec 2023 (estimated)
- Primary completion
- Dec 2024 (estimated)
- Study completion
- Feb 2025 (estimated)
- First posted
- 30 Oct 2023 (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.
Shoulder impingement syndrome (SIS) is responsible for 44% to 60% of medical consultations related to shoulder pain with an approximate prevalence of 70-200 per 1000 adults, which implies a remarkable use of health care resources. The cost for society is high and patients with shoulder disorders account for 20% of all disability due to musculoskeletal disorder. The underlying mechanisms are thought to include inflammation, degeneration of the tendons or bursa, dysfunctional scapulothoracic and glenohumeral mechanics, debilitated scapular musculature, joint capsule irregularities, postural abnormalities of the neck and shoulder, and morphological abnormalities of the relevant skeletal elements. There is a need for well-designed structured exercise program in detail considering content, dosage and progression to guide treatment for patients with sub acromial pain.
The purpose of this study is to develop and validate a structured exercise protocol and to assess its effectiveness in patients with sub-acromial impingement syndrome. Through the extensive literature review, the exercise program would be proposed. In Phase 1, We will develop and validate a structured exercise programs for sub acromial impingement syndrome using an expert consensus Delphi-based survey technique. In phase 2, a randomized controlled trial will be conducted. Group A (Experimental Group) will receive newly structured exercises for twelve weeks and Group B (control group) will receive conventional exercise program for 12 weeks. Evaluation of the participant will be done at the baseline using Constant Murley Score, shoulder pain and disability Index (SPADI). Shoulder range of motion, shoulder muscles extensibility will be assessed and scapulothoracic ratio will be calculated and documented. T-FAST test will be conducted to score the patients functional performance.
Assessment will be done at baseline, 3, 6, 9, and 12 weeks in both the groups. At the end of the study the data will be collected, coded and tabulated using descriptive and inferential statistics.
Detailed description
Shoulder pain is very common with an annual population prevalence of up to 46.7%, and a lifetime prevalence of up to 67%.1 In primary care, shoulder pain is the third most common musculoskeletal presentation. 1, 2 Shoulder pain may have an unfavourable outcome, with only about 50% of all new episodes of shoulder complaints presenting in physiotherapy practice showing a complete recovery within 6 months. Symptoms may be disabling in terms of the patient's ability to carry out daily activities at home and at the workplace. The most frequent shoulder diagnosis is subacromial pain syndrome, affecting about half of all shoulder patients, both in general practice and in secondary care. Shoulder impingement syndrome (SIS) is responsible for 44% to 60% of medical consultations related to shoulder pain implies a remarkable use of health care resources. The cost for society is high and patients with shoulder disorders account for 20% of all disability due to musculoskeletal disorder. The diagnosis of SIS is therefore mainly based on functional aspects and on an affected anatomical structure and requires a thorough history and clinical examination, including aspects such as activity and participation restrictions, aggravating and easing factors, or the "patients' perspective on the situation". Physiotherapy assessment has a very significant role to find out the structural and functional impairments and accordingly set the goals of management. Diagnosing the cause and identifying the source or affected structure is of utmost importance in Physiotherapy management. Apart from focusing only on structures, physiotherapy assessment emphasizes on movement dysfunctions and biomechanical derangements commonly seen in patients with impingement. Correction of the biomechanical faults would off load the sub acromial space and reduce the pain. The technique used to correct the biomechanics is called "load modification or Shoulder symptom modification process" and involves techniques: Alterations to thoracic kyphosis, Scapular positioning techniques, Humeral head positioning procedures and pain and symptom neuromodulation procedure. Current evidence for the physiotherapeutic treatment of SIS, summarized in systematic reviews through the last years, supports the specific and structured exercise program. Furthermore, these studies used either different types of exercises in their groups as a basic treatment, or applied a pre-defined set of manual techniques to all patients without considering the individual situation of the patient. Reasons for the selection or the combination of the exercises or the manual techniques used varied considerably between studies, were often not explained and thus remained unclear. Recent systematic review and meta-analysis conducted by Louis Pieter and Jeremy Lewis in 2020 concluded that continued research is needed to more fully understand the uncertainty around the optimal type, dose, and duration of exercise for sub-acromial shoulder pain. Thus, nearly all current systematic reviews emphasize the need for more high quality trials of physiotherapy interventions to optimize the dosimetry of exercise program. The term conventional physiotherapy is uninterpretable and inconclusive especially because there is presumption of how exactly the exercise program is formed. Many of the exercise program do not provide adequate information of what and why interventions are used. There are many varieties of exercises with different rationale and techniques. Hence, it is mandatory to have an adequate description of techniques making up the intervention and rationale for dosage is essential i.e. the number of sessions, intensity, and duration of intervention as per the TIDieR checklist (Template for Intervention description and replication). There is a need for well-designed structured exercise program in detail considering content, dosage and progression to guide treatment for patients with sub acromial pain. This demands developing a specific guidance on how exercise interventions should be reported in clinical trials depending on what structure is affected in intrinsic and extrinsic mechanisms of subacromial impingement syndrome. 4 The purpose of this study is to develop and validate a structured exercise protocol and to assess its effectiveness in patients with sub-acromial impingement syndrome. Through the extensive literature review, the exercise program would be proposed. We will develop and evaluate a structured exercise programs for sub acromial impingement syndrome using an expert consensus Delphi-based survey technique. Structured exercise program will be formed as per the guidelines of TIDieR items which will include the name of the intervention; intervention rationale for essential elements; intervention materials and details about how to access them; description of the intervention procedures; details of intervention providers; mode of delivery of intervention; location of intervention delivery and key infrastructure; details about the number, duration, intensity, and dose of intervention sessions; details of any intervention tailoring; any intervention modifications throughout the study; and details of intervention assessment, monitoring, and level achieved. This intervention will be based on shoulder kinetic control, load modification exercises and lumbopelvic stabilization with core stability exercises which is not a part of conventional exercise program for shoulder impingement syndrome patients. The study will be conducted in two phases. Phase 1 will be to develop and validate a structured exercise program and phase 2 is to evaluate efficacy of structured exercises on pain, range of motion and shoulder functions using Constant Murley score and Shoulder Pain and Disability Index (SPADI) and functional performance using timed functional arm and shoulder test. A randomized controlled trial will be conducted. Group A (Experimental Group) will receive structured exercises for twelve weeks and Group B (control group) will receive conventional exercise program for 12 weeks. Evaluation of the participant will be done at the baseline using Constant Murley Score, shoulder pain and disability Index (SPADI). Shoulder range of motion, shoulder muscles extensibility will be assessed and scapulothoracic ratio will be calculated and documented. T-FAST test will be conducted to score the patients functional performance. Assessment will be done at baseline, 3, 6, 9, and 12 weeks in both the groups. At the end of the study the data will be collected, coded and tabulated using descriptive and inferential statistics. The data will be analyzed to see the efficacy of newly developed structured exercise program versus conventional exercise program.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Structured exercise group | Experimental | Other: Structured exercise programGroup A (Experimental Group) will receive structured exercises protocol, will be given approximately for two days per week for twelve weeks. |
| Conventional Exercise group | Active comparator | Other: Conventional Exercise ProgramGroup B (control group) will receive conventional exercise program for two days per week for twelve weeks. |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- Age group between 18-60 years
- Symptoms for more than three weeks
- Main complaints in the gleno humeral joint region or the proximal arm
- Presence of one of the following signs indicating SAIS: Neer impingement test, Hawkins-Kennedy impingement test, painful arc with active abduction or flexion. Pain with one of the following resistance tests: external rotation, internal rotation, abduction
Key exclusion criteria (11 listed)
- Severe pain; pain is > 7/10 on NRS (0 = no pain)
- Shoulder surgery on affected shoulder
- Traumatic shoulder dislocation/ fracture within the past 3 months
- Previous rehabilitation for this episode of shoulder pain
- Reproduction of shoulder pain with active or passive cervical motion
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 |
|---|---|---|
| Structured exercise programThis intervention will be based on shoulder kinetic control, load modification exercises and lumbopelvic stabilization with core stability exercises which is not a part of conventional exercise program for shoulder impingement syndrome patients. | Other | Structured exercise group |
| Conventional Exercise ProgramConventional exercise program for shoulder impingement syndrome patients | Other | Conventional Exercise group |
Primary outcome
Constant-Murley Score
Time frame: Baseline, 3, 6, 9, and 12 weeks
This score is a shoulder-specific assessment tool containing objective measures (range of movement and shoulder strength) and subjective measures (activity of daily living and pain). This scale assesses four aspects related to shoulder pathology; two subjective: pain and activities of daily living (ADL) and two objectives: range of motion (ROM) and strength. The subjective components can receive up to 35 points and the objective 65, resulting in a possible maximum total score of 100 points (best function). Pain and ADL are answered by the patient; ROM and strength require a physical evaluation and are answered by the physiotherapist.
Visual analouge Scale
Time frame: Baseline, 3, 6, 9, and 12 weeks
The visual analogue scale (VAS; 0-10) is used to assess the patient's perceived pain intensity at rest, during arm activity and at night during the previous 24 hours at each follow-up. The visual analogue scale (VAS) uses a 10 cm line with endpoint descriptors such as 'no pain' marked at the left end of the line and 'worst pain imaginable' marked at the right end. Patients are asked to mark a point on the line that best represents their pain. The distance from 'no pain' to the patient's mark is then measured and this equals the Visual Analouge scale score.
The Shoulder Pain and Disability Index (SPADI)
Time frame: Baseline, 3, 6, 9, and 12 weeks
The Shoulder Pain and Disability Index is a self-administered questionnaire that consists of two dimensions, one for pain and the other for functional activities. The pain dimension consists of five questions regarding the severity of an individual's pain. Functional activities are assessed with eight questions designed to measure the degree of difficulty an individual has with various activities of daily living that require upper-extremity use. To answer the questions, patients place a mark on a 10cm visual analogue scale for each question. Verbal anchors for the pain dimension are 'no pain at all' and 'worst pain imaginable', and those for the functional activities are 'no difficulty' and 'so difficult it required help'. The scores from both dimensions are averaged to derive a total score. The means of the two subscales are averaged to produce a total score ranging from 0 (best) to 100 (worst).
Timed Functional Arm and Shoulder Test
Time frame: Baseline, 3, 6, 9, and 12 weeks
The Timed Functional Arm and Shoulder Test (TFAST)is a simple battery of physical performance tests for functional task used for shoulder assessment.
1 secondary outcome
Scapulothoracic ratio Measurement
Time frame: Baseline, 3, 6, 9, and 12 weeks
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Oct 2023.
- Results publication: PubMed 10696154Ludewig PM, Cook TM. Alterations in shoulder kinematics and associated muscle activity in people with symptoms of shoulder impingement. Phys Ther. 2000 Mar;80(3):276-91.
- Results publication: PubMed 28416022Shire AR, Staehr TAB, Overby JB, Bastholm Dahl M, Sandell Jacobsen J, Hoyrup Christiansen D. Specific or general exercise strategy for subacromial impingement syndrome-does it matter? A systematic literature review and meta analysis. BMC Musculoskelet Disord. 2017 Apr 17;18(1):158. doi: 10.1186/s12891-017-1518-0.
- Results publication: PubMed 20534140Kromer TO, de Bie RA, Bastiaenen CH. Effectiveness of individualized physiotherapy on pain and functioning compared to a standard exercise protocol in patients presenting with clinical signs of subacromial impingement syndrome. A randomized controlled trial. BMC Musculoskelet Disord. 2010 Jun 9;11:114. doi: 10.1186/1471-2474-11-114.
- Results publication: PubMed 31726927Pieters L, Lewis J, Kuppens K, Jochems J, Bruijstens T, Joossens L, Struyf F. An Update of Systematic Reviews Examining the Effectiveness of Conservative Physical Therapy Interventions for Subacromial Shoulder Pain. J Orthop Sports Phys Ther. 2020 Mar;50(3):131-141. doi: 10.2519/jospt.2020.8498. Epub 2019 Nov 15.
- Results publication: PubMed 22947240Worsley P, Warner M, Mottram S, Gadola S, Veeger HE, Hermens H, Morrissey D, Little P, Cooper C, Carr A, Stokes M. Motor control retraining exercises for shoulder impingement: effects on function, muscle activation, and biomechanics in young adults. J Shoulder Elbow Surg. 2013 Apr;22(4):e11-9. doi: 10.1016/j.jse.2012.06.010. Epub 2012 Sep 1.
- Individual participant dataSharing planned: No
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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.
Reshma Gurav principal investigator
Hamad Medical Corporation
Questions about this trial
What is this clinical trial studying?
A study testing Structured exercise program and Conventional Exercise Program in people with Subacromial Impingement Syndrome, run by Hamad Medical Corporation.
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 11 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 30 Oct 2023. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Reshma Gurav, MPTh (+97455023509, RGurav@hamad.qa), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Constant-Murley Score (time frame: Baseline, 3, 6, 9, and 12 weeks). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06107985, which also lists 5 linked publications.
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 30 Oct 2023; AzTrials last refreshed its copy on 27 Oct 2026.