- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03402867
Effects of Dry Needling on Neck and Shoulder Pain in Orchestral Musicians: a Prospective Case Series
July 5, 2018 updated by: Aitor Martin-Pintado Zugasti, CEU San Pablo University
Effects of Myofascial Trigger Point Dry Needling on Neck Pain in Orchestral Musicians
This study evaluates the effectiveness of Deep dry needling of active myofascial trigger points present in muscles of the neck and shoulder region in orchestral musicians.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
8
Phase
- Phase 2
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Comunidad De Madrid
-
Madrid, Comunidad De Madrid, Spain, 28668
- CEU San Pablo University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Orchestral musicians
- Chronic neck or shoulder pain
- Presence of active myofascial trigger points
Exclusion Criteria:
- Fear of needles
- Coagulation disorders
- Pregnancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Intervention
Deep dry needling applied on active myofascial trigger points in the shoulder and neck regions
|
Insertion of a filiform needle in the active trigger point of musculoskeletal muscle
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual analogue scale for pain
Time Frame: 2 weeks
|
Pain measurement.
100-mm visual analog scale (VAS), horizontal line ranging from 0mm (no pain) to 100mm (worst imaginable pain).
|
2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pressure pain threshold
Time Frame: 2 weeks
|
Analogic algometer
|
2 weeks
|
|
Neck disability index (NDI)
Time Frame: 2 weeks
|
10-item, 50-point index that assesses different aspects of daily functioning in patients with neck pain.
It assesses four items regarding subjective symptoms (pain intensity, headache, concentration, sleeping), four items regarding activities of daily living (lifting, work, driving, recreation), and two items regarding discretionary activities of daily living (personal care, reading).
Each item is scored 0 to 5, with the total reported as either a raw score (0-50) or as a percentage score.
Higher values represent a worse outcome.
|
2 weeks
|
|
Shoulder pain disability index (SPADI)
Time Frame: 2 weeks
|
Self-administered questionnaire, grouping 13 questions, 5 of which measure the severity of pain caused by various arm movements involving the shoulder, the pain being assessed on a numeric pain scale ranging from 0 to 10. Eight additional questions related to functional impairments of the shoulder are assessed with a numeric scale.
Higher values represent a worse outcome.
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
February 1, 2018
Primary Completion (ACTUAL)
March 1, 2018
Study Completion (ACTUAL)
March 5, 2018
Study Registration Dates
First Submitted
January 10, 2018
First Submitted That Met QC Criteria
January 17, 2018
First Posted (ACTUAL)
January 18, 2018
Study Record Updates
Last Update Posted (ACTUAL)
July 6, 2018
Last Update Submitted That Met QC Criteria
July 5, 2018
Last Verified
July 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CEU-012
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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