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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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1 February 2016 |
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Main ID: |
NCT02558686 |
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Date of registration:
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21/09/2015 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Exercise and Post-dry Needling Soreness
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Scientific title:
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Effects of Eccentric Exercise, Sham or Placebo on Post-Needling Soreness by Dry Needling on Active Trigger Points |
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Date of first enrolment:
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October 2015 |
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Target sample size:
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90 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02558686 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Spain
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Contacts
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Name:
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Cesar Fernández-de-las-Peñas, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Universidad Rey Juan Carlos |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Unilateral non-traumatic shoulder pain
- Shoulder pain from at least 6 months
- Shoulder pain of more than 3 points on a NPRS
- Presence of active trigger point in the infraspinatus muscle
Exclusion Criteria:
- bilateral shoulder pain
- younger than 18 or older than 65 years
- shoulder injury
- upper extremity surgery
- fibromyalgia syndrome
- neck or shoulder surgery
- cervical radiculopathy
- whiplash
- any type of intervention for the neck-shoulder the previous year
Age minimum:
18 Years
Age maximum:
65 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Shoulder Pain
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Intervention(s)
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Other: Detuned Ultrasound
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Other: Eccentric Exercise
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Other: Placebo
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Primary Outcome(s)
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Changes in post-dry needling pain intensity before and after the intervention
[Time Frame: Baseline, 24 hours after, 48 hours after and 72 hours after treatment]
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Secondary Outcome(s)
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Changes in disability before and after the intervention
[Time Frame: Baseline and 72 hours after treatment]
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Changes in spontaneous shoulder pain before and after the intervention
[Time Frame: Baseline and 72 hours after treatment]
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Changes in functionality before and after the intervention
[Time Frame: Baseline and 72 hours after treatment]
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Secondary ID(s)
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URJC 2015-12
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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