NCT06603779

Brief Summary

This trial will involve three groups. The Integrated Neuromuscular Inhibition group will receive the integrated neuromuscular inhibition technique. The cervical and Scapular stabilization group will receive cervical and scapular stabilization exercises. The ultrasound group will receive ultrasound therapy

Trial Health

87
On Track

Trial Health Score

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

Enrollment
46

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2024

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

First Submitted

Initial submission to the registry

September 12, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 19, 2024

Completed
12 days until next milestone

Study Start

First participant enrolled

October 1, 2024

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 28, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 28, 2025

Completed
Last Updated

August 26, 2025

Status Verified

August 1, 2025

Enrollment Period

10 months

First QC Date

September 12, 2024

Last Update Submit

August 24, 2025

Conditions

Outcome Measures

Primary Outcomes (4)

  • Visual Analogue Scale (VAS)

    Visual Analogue Scale is a scale that measures pain intensity. Subjects will instructed to indicate their current pain by marking a point on a 10 mm transverse line with 0 degrees meaning "no pain" and 10 meaning the "worst pain"

    1-3 months

  • Pressure Pain Algometer

    The pressure pain Algometer is a device that measures the pain threshold of the subjects.

    1-3 months

  • Neck Pain and Disability Questionnaire (NDI)

    Neck Pain and Disability is a questionnaire that measures neck pain and disabilities in subjects. Each question in the questionnaire will explained in detail and the subject will be asked to select one sentence out of six that best describes their function, a higher score indicates a great loss of function.

    1-3 months

  • 36-item Short-Form Health Questionnaire

    36-item Short-Form Health Questionnaire will measure quality of life

    1-3 months

Study Arms (3)

Integrated Neuromuscular Inhibition Group

EXPERIMENTAL

This group will receive the Integrated Neuromuscular Inhibition Technique which consists of ischemic compression, strain counter strain, and muscle energy technique

Other: Integrated Neuromuscular technique

Cervical and Scapular Stabilization exercises Group

EXPERIMENTAL

This group will receive a group of exercises for the neck and scapula which will strengthen both of them

Ultrasound Therapy Group

PLACEBO COMPARATOR

This group will receive ultrasound Therapy

Device: Ultasound Therapy

Interventions

a device that transmit ultrasound waves to the participant through direct contact

Ultrasound Therapy Group

Integrated Neuromuscular technique is a kind of Manual therapy which include Ischemic Compression, Strain counter-strain and muscle energy technique

Integrated Neuromuscular Inhibition Group

Cervical and Scapular Stabilization exercises are a group of therapeutic exercises.

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients with active trigger points in the upper trapezius for more than 2 weeks based on the Simons Criteria.
  • Age ranged from 18-25 years.
  • Pain intensity ≥ 3 on VAS.
  • Females and males.

You may not qualify if:

  • Patients indicated for surgery.
  • Patients with symptomatic disc lesions.
  • Patients with rheumatological diseases or traumatic neck injury.
  • Patients injected with corticosteroids in the last 6 months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Physical Therapy

Banī Suwayf, Egypt

Location

MeSH Terms

Conditions

Myofascial Pain Syndromes

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
double blind
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of Physical Therapy

Study Record Dates

First Submitted

September 12, 2024

First Posted

September 19, 2024

Study Start

October 1, 2024

Primary Completion

July 28, 2025

Study Completion

July 28, 2025

Last Updated

August 26, 2025

Record last verified: 2025-08

Locations