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Instrument-Assisted Soft Tissue Mobilization as an Adjunct to Therapeutic Exercises in Individuals With Knee Osteoarthritis

Efficacy of Instrument-Assisted Soft Tissue Mobilization as an Adjunct to Therapeutic Exercises in Individuals With Knee Osteoarthritis: A Parallel-Group Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07710209
Enrollment
50
Registered
2026-07-17
Start date
2025-02-01
Completion date
2025-12-31
Last updated
2026-07-17

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

Conditions

Knee Osteoarthritis (OA)

Keywords

Knee osteoarthritis; Instrument-assisted soft tissue mobilization; Therapeutic exercise; Randomized controlled trial; Functional outcomes

Brief summary

To determine the efficacy of IASTM as an adjunct to therapeutic exercises on pain, range of motion, and functional performance in individuals with knee OA.

Detailed description

Background: Knee osteoarthritis (OA) is a leading cause of chronic pain and functional limitation, particularly in older adults, and is associated with soft tissue restrictions, quadriceps weakness, and reduced joint mobility. Therapeutic exercise remains a cornerstone of conservative management, but persistent myofascial restrictions may limit its full benefit. Instrument-Assisted Soft Tissue Mobilization (IASTM) has been proposed as an adjunct technique to address fascial adhesions, improve tissue extensibility, and enhance the outcomes of exercise-based rehabilitation. However, evidence regarding its added value when combined with conventional therapeutic exercise in knee OA remains limited. Objective: To determine the efficacy of IASTM as an adjunct to therapeutic exercises on pain, range of motion, and functional performance in individuals with knee OA. Methodology: A parallel-group randomized controlled trial was conducted on 50 participants diagnosed with knee OA (Kellgren-Lawrence grade II-III), randomly allocated into two equal groups (n=25 each) using a computer-generated random sequence with allocation concealment. Group A received IASTM combined with a standardized therapeutic exercise protocol, while Group B received the therapeutic exercise protocol alone. Treatment was administered three times per week for 6 weeks. Outcome measures included the Numeric Pain Rating Scale (NPRS), Knee range of motion (goniometry), and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) for functional status, assessed at baseline and post-intervention (6 weeks). Data were analyzed using paired and independent sample t-tests, with significance set at p\<0.05.

Interventions

BEHAVIORALIATSM

IATSM were administered for a duration of 6 weeks

BEHAVIORALTherapeutic Exercise

Therapeutic Exercise were administered for a duration of 6 weeks

Sponsors

Foundation of Medical Research and Laboratories, Pakistan
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Osteoarthritis, both gender, Age between 40-60 years. -

Exclusion criteria

Not meeting the inclusion criteria, underwent recent surgery of lower limb. \-

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rating Scale (NPRS)6 weeksThe value were taken at base line and after 6 weeks of intervention
Knee range of motion (goniometry)6 weeksThe value were taken at base line and after 6 weeks of intervention
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)6 weeksThe value were taken at base line and after 6 weeks of intervention

Countries

Pakistan

Contacts

STUDY_DIRECTORMalika Hassan

fmr.labs@medicalresearchforum.net

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 18, 2026