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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03402867
Other study ID # CEU-012
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received
Last updated
Start date February 1, 2018
Est. completion date March 5, 2018

Study information

Verified date July 2018
Source CEU San Pablo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date March 5, 2018
Est. primary completion date March 1, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Orchestral musicians

- Chronic neck or shoulder pain

- Presence of active myofascial trigger points

Exclusion Criteria:

- Fear of needles

- Coagulation disorders

- Pregnancy

Study Design


Intervention

Procedure:
Deep dry needling
Insertion of a filiform needle in the active trigger point of musculoskeletal muscle

Locations

Country Name City State
Spain CEU San Pablo University Madrid Comunidad De Madrid

Sponsors (1)

Lead Sponsor Collaborator
CEU San Pablo University

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual analogue scale for pain Pain measurement. 100-mm visual analog scale (VAS), horizontal line ranging from 0mm (no pain) to 100mm (worst imaginable pain). 2 weeks
Secondary Pressure pain threshold Analogic algometer 2 weeks
Secondary Neck disability index (NDI) 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
Secondary Shoulder pain disability index (SPADI) 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
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