RecruitingNot ApplicableNCT07685340

Dry Dynamic Cupping vs Instrument-Assisted Soft Tissue Mobilization for Chronic Myofascial Low Back Pain

Comparative Effects of Dry Dynamic Cupping and Instrument-Assisted Soft Tissue Mobilization in Patients With Chronic Myofascial Low Back Pain


Sponsor

Ibadat International University, Islamabad

Enrollment

48 participants

Start Date

Jan 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to compare the effects of Dry Dynamic Cupping and Instrument-Assisted Soft Tissue Mobilization (IASTM) in patients with chronic myofascial low back pain. The interventions will be evaluated for their effectiveness in reducing pain, improving functional disability, and enhancing quality of life. The findings may help identify a more effective treatment approach for managing chronic myofascial low back pain.


Eligibility

Min Age: 25 YearsMax Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Instrument Assisted Soft Tissue Mobilization (IASTM) and dry cupping for people with chronic myofascial low back pain. The study is currently recruiting participants at 1 location. People eligible for this study include aged 25 Years to 45 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERInstrument Assisted Soft Tissue Mobilization (IASTM)

Participants in this group will receive Instrument-Assisted Soft Tissue Mobilization (IASTM). The intervention will be administered for 2 weeks, with 3 treatment sessions per week, according to the standardized study protocol. The effects of the intervention will be evaluated on pain intensity, functional disability, and lumbar range of motion.

OTHERdry cupping

Participants in this group will receive Dry Dynamic Cupping therapy. The intervention will be administered for 2 weeks, with 3 treatment sessions per week, according to the standardized study protocol. The effects of the intervention will be evaluated on pain intensity, functional disability, and lumbar range of motion.


Locations(1)

Mediplex Healthcare Center, Rawalpindi

Rawalpindi, Punjab Province, Pakistan

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NCT07685340