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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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07685340
Enrollment
48
Registered
2026-07-06
Start date
2026-01-01
Completion date
2026-09-01
Last updated
2026-07-06

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

Conditions

Chronic Myofascial Low Back Pain

Keywords

chronic, myofascial, back pain, low back, low back pain, backache

Brief 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.

Interventions

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.

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.

Sponsors

Ibadat International University, Islamabad
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
25 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Chronic Myofascial Lower Back Pain \> 3 months * Pain reproduced by palpation of Lumbar Para-Spinals, Quadratus Lumborum (QL) or Thoracolumbar Fascia. * Trigger Points will be diagnosed through Simons and Travell's Criteria * Age 25-45 years (young adults according to WHO classification) * Both genders

Exclusion criteria

* History of spinal surgery * Presence of inflammatory or neurological disorders * Facet joint dysfunction * Discogenic pain * Ligamentous pain * Pregnant females

Design outcomes

Primary

MeasureTime frameDescription
NPRSBaseline and 2 Weeks Post-InterventionPain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), an 11-point scale ranging from 0 (no pain) to 10 (worst imaginable pain). Changes in pain scores will be compared between the Dry Dynamic Cupping and IASTM groups.

Secondary

MeasureTime frameDescription
ODIBaseline and 2 Weeks Post-InterventionFunctional disability related to low back pain will be assessed using the Oswestry Disability Index (ODI). Changes in disability scores will be compared between groups.

Countries

Pakistan

Contacts

CONTACTMUHAMMAD ASHAR RAFI, DPT, MS-NMPT
ashar.rafi@uipt.iiui.edu.pk0092-308-3407837
CONTACTMUHAMMAD ARBAZ KHAN, DPT
arbazkhantastic3@gmail.com0092-333-9001698
PRINCIPAL_INVESTIGATORMUHAMMAD ASHAR RAFI, DPT, MS-NMPT

IBADAT INTERNATIONAL UNIVERSITY

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 7, 2026