Efficacy of Dry Needling in Cervical Pain

Sponsor
Universidad Católica de Ávila (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05624515
Collaborator
(none)
80
1
2
1.5
54.1

Study Details

Study Description

Brief Summary

The presence of latent myofascial trigger points (MTrPs) in the angular muscle of the scapula is one of the possible causes of non-specific neck pain. Dry needling (DN) and ischaemic compression (IC) techniques may be useful for the treatment of these MTrPs. Methods: 80 participants were divided into two groups: the dry needling group, which received a single session of DN on the angular muscle plus hyperalgesia (n=40), and the IC group, which received a single session of IC on the angular muscle plus hyperalgesia (n=40). Pain intensity, pain pressure threshold (PPT), range of motion (ROM) and quality of life were assessed at baseline, immediately after, 48 hours and one week after treatment.

Condition or Disease Intervention/Treatment Phase
  • Device: dry needling
  • Other: Ischaemic compression
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Health Services Research
Official Title:
Efficacy of Dry Needling and Ischaemic Compression of the Scapula Angularis Muscle in Patients With Cervicalgia. Randomised Clinical Trial
Anticipated Study Start Date :
Dec 1, 2022
Anticipated Primary Completion Date :
Jan 1, 2023
Anticipated Study Completion Date :
Jan 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: dry needling group

Subjects undergoing dry needling of the angularis scapulae muscle

Device: dry needling
Active trigger point puncture of the angularis scapulae muscle

Experimental: ischaemic compression group

Subjects undergoing ischaemic compression of the angularis scapulae muscle

Other: Ischaemic compression
Ischaemic compression at the active trigger point of the angularis scapulae muscle

Outcome Measures

Primary Outcome Measures

  1. Pain intensity [3 months]

    Pain intensity measured on the VAS scale with a minimum score of 0 (no pain) and a maximum score of 10 (highest possible pain endured).

Secondary Outcome Measures

  1. pressure pain threshold [3 months]

    pressure on the sore spot measured by algometer and the unit is Newtons.

  2. range of motion [3 months]

    Joint movement in the cervical spine measured in degrees using a goniometer

  3. quality of life [3 months]

    Measured by physical activity questionnaire. Scoring is based on patients' responses. Minimum of 0, maximum of 100 points.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients presenting with neck pain

  • Patients presenting with trigger point activation of the angularis scapulae muscle

Exclusion Criteria:
  • Patients who have an absolute fear of needles (belonephobia).

  • Patients presenting with cervical pain with radiculopathy or irradiation of pain to the upper limb.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Universidad Católica de Ávila Ávila Completado Spain 05005

Sponsors and Collaborators

  • Universidad Católica de Ávila

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
JORGE VELAZQUEZ SAORNIL, Principal Investigator, Universidad Católica de Ávila
ClinicalTrials.gov Identifier:
NCT05624515
Other Study ID Numbers:
  • 14/11/2022
First Posted:
Nov 22, 2022
Last Update Posted:
Nov 22, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by JORGE VELAZQUEZ SAORNIL, Principal Investigator, Universidad Católica de Ávila
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 22, 2022