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Neuromuscular Reeducation on Myofascial Trigger Point

Effect of Neuromuscular Reeducation on Myofascial Trigger Point in Cervical Pain patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190924044861N1
Enrollment
70
Registered
2019-09-27
Start date
2017-01-05
Completion date
Unknown
Last updated
2019-11-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cervical pain due to myofascial trigger points(MTRPs). Other soft tissue disorders related to use, overuse and pressure

Interventions

Intervention 1: Control group:Moist HOT PACK: (5-8mins) at the start of treatment 2. Ultrasound: Frequency:1- 3 MHz, Intensity:1- 1.4 W/cm2, Time: 8-10 minutes,3. Ischemic compression: Appropriate a

Sponsors

RIPHAH COLLEGE OF REHABILITATION SCIENCES,ISLAMABAD,PAKISTAN
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Pain more than 5 on NPRS Reduced cervical lateral flexion to the opposite side and Painful upper trapezius trigger point Hypersensitive taut band in Upper fiber of trapezius Jump sign identification through patient vocalization or withdrawal symptom

Exclusion criteria

Exclusion criteria: Recent traumatic history of cervical spine or shoulder region Diagnosed Fibromyalgia syndrome Whiplash injury Malignancy Skin infections or open wound in the site of upper trapezius

Design outcomes

Primary

MeasureTime frame
Goniometer for upper trapezius Range of motion(muscle length). Timepoint: before intervention and after 2 weeks of intervention. Method of measurement: Goniometer for upper trapezius Range of motion(muscle length)placed goniometer in upper fibers of trapezius and ask to perform the movement, measure the ROM and then compare it with intact side.

Secondary

MeasureTime frame
Numeric Pain rating Scale(NPRS) for pain assessment scores. Timepoint: NPRS scores before treatment than after 2 weeks of treatment. Method of measurement: NPRS score beyond 5 were assessed before intervention and compare it after 2 weeks.

Countries

Pakistan

Contacts

Public ContactKinza Anwar

The University of Lahore,Islamabad Campus,Pakistan

kinza.anwar29@gmail.com+92 51 5537867

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026