NCT05870904

Brief Summary

This randomized control trial was conducted to investigate the efficacy of trigger point dry needling which is a modern treatment intervention compared with ischemic compression release in the patients having neck pain due to myofascial trigger points.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2021

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2021

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 31, 2021

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

April 26, 2023

Completed
27 days until next milestone

First Posted

Study publicly available on registry

May 23, 2023

Completed
Last Updated

May 23, 2023

Status Verified

May 1, 2023

Enrollment Period

4 months

First QC Date

April 26, 2023

Last Update Submit

May 13, 2023

Conditions

Keywords

Dry NeedlingIschemic CompressionNeck Pain

Outcome Measures

Primary Outcomes (2)

  • Change in Pain assessed through Visual Analogue Pain Scale

    To measure the change in terms of betterment or aggravation in the intensity of pain baseline then after week 1,week 2 and after week 3.

    Data was Collected at Baseline and after week 1,2 & 3.

  • Change in degree of disability assessed through Northwick Park Neck Pain Questionnaire.

    To measure change in the intensity of neck pain and the consequent patient disabilities at baseline then after week 1,week 2 and after week 3.

    Data was Collected at Baseline and after week 1,2 & 3.

Study Arms (2)

Dry Needling Group

EXPERIMENTAL

Received dry needling through the insertion of fusiform needle for the trigger point release on 3 days a week aimed at pain relief.

Other: Dry Needling

Ischemic Compression Group

ACTIVE COMPARATOR

Received ischemic compression release through thumb pressure for trigger points on 3 days a week.

Other: Dry Needling

Interventions

Dry Needling includes the insertion of a fine, strong filiform needle without presentation of any pain relieving medicine. Ischemic pressure is usually applied to trigger point, in what is known as trigger point therapy, where enough continuous pressure is applied to a trigger point within a tolerable measure of pain, and as discomfort is decreased, extra pressure is gradually applied

Also known as: Ischemic Compression
Dry Needling GroupIschemic Compression Group

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients between the age group of 20 to 40 years.
  • Both Male and female patients.
  • Patients presenting with neck pain due to MTrP's.
  • The presence of a palpable taut band in the neck region.
  • Patients reporting typically referred pain pattern of the MTrP in response to compression.

You may not qualify if:

  • Patients with any associated comorbidities such as hypertension and diabetes.
  • Patients with known history of fibromyalgia syndrome, whiplash injury, cervical spine surgery fracture and cervical radiculopathy.
  • Patients with any systemic disease such as rheumatism and tuberculosis or cervical myelopathy and multiple sclerosis.
  • Patients with history of myofascial trigger point therapy one month prior to enrollment.
  • Patients with non-cooperative attitude, fear or any contraindications to needling.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bashir Institute of Health Sciences,Bashir General & Dental Hospital

Islamabad, 45400, Pakistan

Location

MeSH Terms

Conditions

Neck PainMyofascial Pain Syndromes

Interventions

Dry NeedlingAcupressure

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsMuscular DiseasesMusculoskeletal Diseases

Intervention Hierarchy (Ancestors)

Complementary TherapiesTherapeuticsPhysical Therapy ModalitiesTherapy, Soft TissueMusculoskeletal ManipulationsRehabilitation

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Senior Lecturer

Study Record Dates

First Submitted

April 26, 2023

First Posted

May 23, 2023

Study Start

June 1, 2021

Primary Completion

September 30, 2021

Study Completion

October 31, 2021

Last Updated

May 23, 2023

Record last verified: 2023-05

Data Sharing

IPD Sharing
Will not share

Locations