Trial · NCT07885215
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Shoulder Pain and Disability Index (SPADI) Score | Baseline and 3 weeks after baseline | Shoulder pain and disability will be assessed using the Shoulder Pain and Disability Index (SPADI). The SPADI consists of 13 items divided into two subscales: pain (5 items) and disability (8 items). The total score ranges from 0 to 100, with higher scores indicating greater pain and disability. Assessments will be performed at baseline and at the end of the three-week intervention. |
| Secondary | Change in Shoulder Pain Intensity (VAS) | Baseline and 3 weeks after baseline | Pain intensity at rest, during activity, and at night, measured using a 0-10 cm Visual Analog Scale. Higher values indicate greater pain. |
| Secondary | Change in Pulmonary Function (FVC) | Baseline and 3 weeks after baseline | Forced vital capacity measured by spirometry, expressed in liters. |
| Secondary | Change in Pulmonary Function (FEV1) | Baseline and 3 weeks after baseline | Forced expiratory volume in one second, measured by spirometry, expressed in liters. |
| Secondary | Change in FEV1/FVC Ratio | Baseline and 3 weeks after baseline | Ratio of forced expiratory volume in one second to forced vital capacity, expressed as a percentage. |
| Secondary | Change in Peak Expiratory Flow (PEF) | Baseline and 3 weeks after baseline | Peak expiratory flow measured using spirometry. |
| Secondary | Change in Shoulder Range of Motion | Baseline and 3 weeks after baseline | Active and passive shoulder range of motion measured using a universal goniometer, expressed in degrees. |
| Secondary | Change in Modified Constant-Murley Score | Baseline and 3 weeks after baseline | Shoulder pain, daily activities, range of motion, and strength assessed on a 0-100 scale. Higher scores indicate better shoulder function. |
| Secondary | Change in Western Ontario Shoulder Instability Index (WOSI) Score | Baseline and 3 weeks after baseline | The Western Ontario Shoulder Instability Index (WOSI) will be used to assess shoulder-related physical symptoms, sports/recreation/work, lifestyle, and emotional functioning. The questionnaire consists of 21 items, with a total score ranging from 0 to 2100. Higher scores indicate greater shoulder-related impairment and poorer quality of life. |
| Secondary | Change in Pittsburgh Sleep Quality Index (PSQI) | Baseline and 3 weeks after baseline | Sleep quality assessed using the PSQI global score, ranging from 0 to 21. Higher scores indicate poorer sleep quality. |
| Secondary | Change in Pectoral Muscle Shortness | Baseline and 3 weeks after baseline | Pectoral muscle shortness measured using anatomical landmark distances, expressed in centimeters. |
| Secondary | Change in Cervical and Lumbar Range of Motion | Baseline and 3 weeks after baseline | Cervical and lumbar range of motion measured using goniometry, expressed in degrees. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
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GET https://conductscience.org/api/trials/v1/NCT07885215/registered