Dry Needling of the Trapezius Muscle in Office Workers With Neck Pain
Primary Purpose
Myofascial Trigger Point Pain
Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Group 1. Deep dry needling
group 2. Passive analitical stretch (performed in both groups)
Sponsored by
About this trial
This is an interventional treatment trial for Myofascial Trigger Point Pain focused on measuring Myofascial pain syndromes,physiotherapy,muscle stretching exercises,neck pain,dry needling
Eligibility Criteria
Inclusion Criteria:
- over 18
- present myofascial trigger points in trapezius muscle
Exclusion Criteria:
- to be under anti-inflammatory, analgesic, anticoagulant, muscle relaxant or antidepressant medication at the start of the study or one week before it (Simons, 2004)
- to suffer from fibromyalgia syndrome, or to have any contraindication to conservative or invasive physiotherapy (infection, fever, hypothyroidism, fear of needles, wounds in the area of the puncture, metal allergy, cancer, systemic disease) (Baldry, 2005).
Sites / Locations
- UDAIF
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Other
Arm Label
Deep dry needling
muscle stretch
Arm Description
The group of DDN receive this treatment and stretch
The stretch applied was as described by Simons et al. (Simons et al., 1999). During the stretch the physiotherapist took up the slack, avoiding pain elicitation, maintaining the tension for four seconds and releasing the tension for eight seconds; this cycle was repeated three times
Outcomes
Primary Outcome Measures
Subjective Pain scored by Visual Analogue Scale (VAS.Participants were followed for the duration of the intervention, an average of 6 weeks)
pretreatment = at baseline; post-treatment= after 5 physical therapy sessions, 3 weeks after baseline; follow-up= 15 days after last intervention.
Secondary Outcome Measures
Pain Pressure Threshold (PPT. Participants were followed for the duration of the intervention, an average of 6 weeks)
pretreatment = at baseline; post-treatment= after 5 physical therapy sessions, 3 weeks after baseline; follow-up= 15 days after last intervention.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02219386
Brief Title
Dry Needling of the Trapezius Muscle in Office Workers With Neck Pain
Official Title
Dry Needling of the Trapezius Muscle in Office Workers With Neck Pain. Randomised, Single Blinded Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
January 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alcala
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Deep dry needling of active myofascial trigger points of trapezius muscle is effective in the dimminution of pain of patients
Detailed Description
EVALUATION:
A blind assesor does a complete evaluation of the patients to determine if they take part of the study. An assesment of pain (by visual analogue scale), Pain pressure theshold (kg/cm2 by algometry, Range of motion (CROM goniometer in degrees) and strength (digital dinamometry in Newtons) are performed. In this evaluation inclusion criteria is checked too.
INTERVENTION:
-TREATMENT GROUP(Deep dry needling group (DDN)):
An experienced physical therapist performed this treatment. The intervention included DDN of every active MTrP found in the trapezius muscle using a 4 cm x 0.32 mm acupuncture needle with guided tube. ). In the case of upper trapezius active MTrPs, DDN was performed in the prone position. For medium and lower trapezius muscle MTrPs, DDN was performed in a side-lying position as described by Simons et al. (Simons et al., 1999). Once the needle was inserted into the MTrP previously marked by the blinded assessor, local twitch responses (LTRs) were obtained by using Hong's fast-in and fast-out technique, which involves rapid movements of the needle in and out of the MTrP.
After that, the stretch is performed
- Passive stretch of the trapezius muscle (both groups)
Another experienced physical therapist, after taking part of training-sesions to do the same stretch as in DDN group, performed the stretch.Participants in this group received the same stretch as patients in treatment group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myofascial Trigger Point Pain
Keywords
Myofascial pain syndromes,physiotherapy,muscle stretching exercises,neck pain,dry needling
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
44 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Deep dry needling
Arm Type
Active Comparator
Arm Description
The group of DDN receive this treatment and stretch
Arm Title
muscle stretch
Arm Type
Other
Arm Description
The stretch applied was as described by Simons et al. (Simons et al., 1999). During the stretch the physiotherapist took up the slack, avoiding pain elicitation, maintaining the tension for four seconds and releasing the tension for eight seconds; this cycle was repeated three times
Intervention Type
Other
Intervention Name(s)
Group 1. Deep dry needling
Intervention Description
Deep dry needling and stretch. The intervention included DDN of every active MTrP found in the trapezius muscle using a 4 cm x 0.32 mm acupuncture needle as described by Simons et al. (Simons et al., 1999). Once the needle was inserted into the MTrP previously marked by the blinded assessor, local twitch responses (LTRs) were obtained by using Hong's fast-in and fast-out technique, which involves rapid movements of the needle in and out of the MTrP. After four LTRs, the needle was withdrawn and the area was disinfected with alcohol again (Simons et al., 1999). Then, passive stretch was performed on the trapezius muscle.
Intervention Type
Other
Intervention Name(s)
group 2. Passive analitical stretch (performed in both groups)
Other Intervention Name(s)
only the same stretch as performed in deep dry needling group.
Primary Outcome Measure Information:
Title
Subjective Pain scored by Visual Analogue Scale (VAS.Participants were followed for the duration of the intervention, an average of 6 weeks)
Description
pretreatment = at baseline; post-treatment= after 5 physical therapy sessions, 3 weeks after baseline; follow-up= 15 days after last intervention.
Time Frame
pretreatment, postreatment and follow-up(15 days)
Secondary Outcome Measure Information:
Title
Pain Pressure Threshold (PPT. Participants were followed for the duration of the intervention, an average of 6 weeks)
Description
pretreatment = at baseline; post-treatment= after 5 physical therapy sessions, 3 weeks after baseline; follow-up= 15 days after last intervention.
Time Frame
Pretreatment, post treatment and follow-up.
Other Pre-specified Outcome Measures:
Title
Strenght scored by Digital dynamometer (Participants were followed for the duration of the intervention, an average of 6 weeks)
Description
pretreatment = at baseline; post-treatment= after 5 physical therapy sessions, 3 weeks after baseline; follow-up= 15 days after last intervention.
Time Frame
Pretreatment, post treatment and follow-up.
Title
Cervical Range of Motion assesed with CROM goniometer (Participants were followed for the duration of the intervention, an average of 6 weeks)
Description
pretreatment = at baseline; post-treatment= after 5 physical therapy sessions, 3 weeks after baseline; follow-up= 15 days after last intervention. Participants were followed for the duration of the intervention, an average of 6 weeks)
Time Frame
Pretreatment, post treatment and follow-up.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
over 18
present myofascial trigger points in trapezius muscle
Exclusion Criteria:
to be under anti-inflammatory, analgesic, anticoagulant, muscle relaxant or antidepressant medication at the start of the study or one week before it (Simons, 2004)
to suffer from fibromyalgia syndrome, or to have any contraindication to conservative or invasive physiotherapy (infection, fever, hypothyroidism, fear of needles, wounds in the area of the puncture, metal allergy, cancer, systemic disease) (Baldry, 2005).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ester Cerezo-Téllez, PT
Organizational Affiliation
Alcalá University
Official's Role
Principal Investigator
Facility Information:
Facility Name
UDAIF
City
Alcalá de Henares
State/Province
Madrid
ZIP/Postal Code
28820
Country
Spain
12. IPD Sharing Statement
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Dry Needling of the Trapezius Muscle in Office Workers With Neck Pain
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