Immediate Effect of Dry Needling on Trigger Points
Primary Purpose
Shoulder Pain
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Dry needling
Sponsored by
About this trial
This is an interventional treatment trial for Shoulder Pain focused on measuring myofascial trigger points,, dry needling,, stiffness
Eligibility Criteria
Inclusion Criteria:
- present with chronic shoulder pain of non-traumatic origin (rated at least 2/10 on a numeric rating scale (NRS) for more than 3 months. The pain had to be located in the shoulder area or referred in the area of the infraspinatus as described by Travell and Simons (1999);
- have a hyperirritable spot within a palpable tight band that reproduced the participant's pain when compressed by palpation; and
- have a body mass index (BMI) lower than 28
Exclusion Criteria:
- diagnosis of capsulitis, cancer, or metastasis;
- previous shoulder or thorax surgery or a mastectomy;
- shoulder girdle bone fracture;
- C4-C5 or C6 radiculopathy;
- known osteoporotic profile (positive bone densitometry);
- apparent atrophy of the infraspinatus fossa (visual interpretation) and
- contraindications to receive a DN intervention
Sites / Locations
- CRCHUS-Physius Lab
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Dry needling of a trigger point in the infraspinatus muscle
Arm Description
Insertion a a acupuncture type needle into a trigger point in the infraspinatus muscle on the painful side to decrease the stiffness and tone and increase the elasticity
Outcomes
Primary Outcome Measures
Tone in Hertz measured with a myotonometer on the trigger point
Measurement of the tone in Hz with the myotonometer MyotonPro on the trigger point
Tone in Hertz measured with a myotonometer on the trigger point
Measurement of the tone in Hz with the myotonometer MyotonPro on the trigger point
Tone in Hertz measured with a myotonometer on the trigger point
Measurement of the tone in Hz with the myotonometer MyotonPro on the trigger point
Stiffness in N/m with a myotonometer on the trigger point
Measurement of the stiffness in N/m with the myotonometer MyotonPro on the trigger point
Stiffness in N/m with a myotonometer on the trigger point
Measurement of the stiffness in N/m with the myotonometer MyotonPro on the trigger point
Stiffness in N/m with a myotonometer on the trigger point
Measurement of the stiffness in N/m with the myotonometer MyotonPro on the trigger point
Elasticity (no units: inversely proportional to the decrement of the oscillations) with a myotonometer on the trigger point
Measurement of the elasticity with the MyotonPro
Elasticity (no units: inversely proportional to the decrement of the oscillations) with a myotonometer on the trigger point
Measurement of the elasticity with the MyotonPro
Elasticity (no units: inversely proportional to the decrement of the oscillations) with a myotonometer on the trigger point
Measurement of the elasticity with the MyotonPro
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04476381
Brief Title
Immediate Effect of Dry Needling on Trigger Points
Official Title
Immediate Effect of Dry Needling on the Viscoelastic Properties of a Trigger Point on the Infraspinatus Muscle Measured With the MyotonPro
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
February 1, 2018 (Actual)
Primary Completion Date
June 7, 2018 (Actual)
Study Completion Date
September 20, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Université de Sherbrooke
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The immediate effects (0-30 minutes) of a dry needling intervention on a trigger point on their viscoelastic properties (tone, elasticity and stiffness)
Detailed Description
Objectives: To investigate the immediate effects of a dry needling puncture on the viscoelastic properties (tone, stiffness and elasticity) of a trigger point (TP) located in the infraspinatus muscle in participants with non-traumatic chronic shoulder pain.
Methods: Forty-eight individuals who presented non-traumatic chronic shoulder pain were recruited. The presence of a TP in the infraspinatus muscle of the painful side was confirmed by an experienced physiotherapist with a palpatory exam according to Travell and Simons criteria. The TP was marked and the viscoelastic properties including tone, stiffness and elasticity were measured with the MyotonPro device by an evaluator. After the first set of measurements (T1), an experienced physiotherapist applied a dry needling puncture to the TP with a pistoning technique to obtain a local twitch response (LTR) with an Optimed 40 x 0.30 mm single use acupuncture needle. The same set of measurements was repeated immediately after the dry needling (T2) and 30 minutes later (T3). Repeated measures ANOVA and post-hoc tests were used to assess changes in viscoelastic properties over time with a significant level set at 0.05.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Shoulder Pain
Keywords
myofascial trigger points,, dry needling,, stiffness
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
One group, one measurement of the viscoelastic properties with the MyotonPro of a single trigger point before the dry needle insertion, one measurement with the MyotonPro right after and 30 minutes later
Masking
None (Open Label)
Allocation
N/A
Enrollment
48 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Dry needling of a trigger point in the infraspinatus muscle
Arm Type
Experimental
Arm Description
Insertion a a acupuncture type needle into a trigger point in the infraspinatus muscle on the painful side to decrease the stiffness and tone and increase the elasticity
Intervention Type
Procedure
Intervention Name(s)
Dry needling
Intervention Description
Insertion of a Optimed 40mm x 0.30 single use, sterile acupuncture needle into a active trigger point in the infraspinatus muscle
Primary Outcome Measure Information:
Title
Tone in Hertz measured with a myotonometer on the trigger point
Description
Measurement of the tone in Hz with the myotonometer MyotonPro on the trigger point
Time Frame
baseline
Title
Tone in Hertz measured with a myotonometer on the trigger point
Description
Measurement of the tone in Hz with the myotonometer MyotonPro on the trigger point
Time Frame
immediately after the intervention
Title
Tone in Hertz measured with a myotonometer on the trigger point
Description
Measurement of the tone in Hz with the myotonometer MyotonPro on the trigger point
Time Frame
30 minutes after the intervention
Title
Stiffness in N/m with a myotonometer on the trigger point
Description
Measurement of the stiffness in N/m with the myotonometer MyotonPro on the trigger point
Time Frame
baseline
Title
Stiffness in N/m with a myotonometer on the trigger point
Description
Measurement of the stiffness in N/m with the myotonometer MyotonPro on the trigger point
Time Frame
immediately after the intervention
Title
Stiffness in N/m with a myotonometer on the trigger point
Description
Measurement of the stiffness in N/m with the myotonometer MyotonPro on the trigger point
Time Frame
30 minutes after the intervention
Title
Elasticity (no units: inversely proportional to the decrement of the oscillations) with a myotonometer on the trigger point
Description
Measurement of the elasticity with the MyotonPro
Time Frame
baseline
Title
Elasticity (no units: inversely proportional to the decrement of the oscillations) with a myotonometer on the trigger point
Description
Measurement of the elasticity with the MyotonPro
Time Frame
immediately after the intervention
Title
Elasticity (no units: inversely proportional to the decrement of the oscillations) with a myotonometer on the trigger point
Description
Measurement of the elasticity with the MyotonPro
Time Frame
30 minutes after the intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
present with chronic shoulder pain of non-traumatic origin (rated at least 2/10 on a numeric rating scale (NRS) for more than 3 months. The pain had to be located in the shoulder area or referred in the area of the infraspinatus as described by Travell and Simons (1999);
have a hyperirritable spot within a palpable tight band that reproduced the participant's pain when compressed by palpation; and
have a body mass index (BMI) lower than 28
Exclusion Criteria:
diagnosis of capsulitis, cancer, or metastasis;
previous shoulder or thorax surgery or a mastectomy;
shoulder girdle bone fracture;
C4-C5 or C6 radiculopathy;
known osteoporotic profile (positive bone densitometry);
apparent atrophy of the infraspinatus fossa (visual interpretation) and
contraindications to receive a DN intervention
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nathaly Gaudreault, PhD
Organizational Affiliation
Université de Sherbrooke
Official's Role
Study Director
Facility Information:
Facility Name
CRCHUS-Physius Lab
City
Sherbrooke
State/Province
Quebec
ZIP/Postal Code
J1H5N4
Country
Canada
12. IPD Sharing Statement
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Immediate Effect of Dry Needling on Trigger Points
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