NCT05816161

Brief Summary

to findout the improvement by Integrated Neuromuscular Inhibition Technique and Myofascial Release on Cervical Range of Motion and Dysfunction

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2023

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

April 3, 2023

Completed
15 days until next milestone

First Posted

Study publicly available on registry

April 18, 2023

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2023

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2023

Completed
Last Updated

April 18, 2023

Status Verified

April 1, 2023

Enrollment Period

2 months

First QC Date

April 3, 2023

Last Update Submit

April 3, 2023

Conditions

Myofascial Trigger Point Pain

Outcome Measures

Primary Outcomes (1)

  • Cervical Range of Motion measurement

    6 Months

Study Arms (2)

Neuromuscular Inhibition Technique

EXPERIMENTAL
Diagnostic Test: Integrated Neuromuscular Inhibition Technique

Myofascial Release

OTHER
Diagnostic Test: Myofascial Release

Interventions

Integrated Neuromuscular Inhibition TechniqueDIAGNOSTIC_TEST

Exercises

Neuromuscular Inhibition Technique
Myofascial ReleaseDIAGNOSTIC_TEST

Exercises

Myofascial Release

Eligibility Criteria

Age25 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • ● Age between 25-40
  • Both males and females included
  • Participants suffering from recent cervical pain without any pathology.

You may not qualify if:

  • ● Participants having cervical radiculopathy
  • Having recent trauma of the cervical spine
  • Non-cooperative subject

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Chaudhary Muhammad Akram Hospital

Lahore, Punjab Province, Pakistan

Location

MeSH Terms

Conditions

Myofascial Pain Syndromes

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

April 3, 2023

First Posted

April 18, 2023

Study Start

April 1, 2023

Primary Completion

June 1, 2023

Study Completion

August 31, 2023

Last Updated

April 18, 2023

Record last verified: 2023-04

Data Sharing

IPD Sharing
Will not share

Locations

PA(1)