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Effects Of Instrument Assisted Soft Tissue Mobilization as Compared With Manual Longitudinal Friction Massage in Individuals With Plantar Fasciitis.

Effects Of Instrument Assisted Soft Tissue Mobilization as Compared With Manual Longitudinal Friction Massage in Individuals With Plantar Fasciitis.

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07614672
Acronym
IMPACT-PF
Enrollment
56
Registered
2026-05-29
Start date
2026-06-22
Completion date
2026-12-30
Last updated
2026-05-29

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

Conditions

Plantar Fasciitis of Both Feet

Keywords

Plantar Fasciitis

Brief summary

This Randomized Controlled Trial aims to compare the effects of instrument assisted soft tissue mobilization(IASTM) and Manual Longitudinal friction massage (MLFM) on pain, functional ability and gait in individuals with plantar fasciitis.

Interventions

Instrument assisted soft tissue mobilization (IASTM) to the plantar fascia and intrinsic foot muscles using longitudinal and sweeping strokes from the calcaneal insertion towards the forefoot.

PROCEDUREManual Longitudinal Friction Massage

Manual longitudinal friction massage that will be applied manually using thumbs or fingers from the calcaneal insertion towards the forefoot.

Sponsors

Ibadat International University, Islamabad
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
19 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

inclusion criteria individuals with the presence of heel pain with first steps in the morning or after prolonged rest, tenderness at medial calcaneal tubercle and positive windlass test individuals with symptoms greater than or equal to 6 weeks Adults and middle-aged adults (19 to 64 years) both males and females participants with BMI less than 35 kg/m2 individuals willing to participate and provide informed consent -

Exclusion criteria

any surgery or fracture at lower extremity any neoplastic growth at foot any neurological or vascular disorders affecting gait participants using foot orthoses such as insoles, heel pads, arch support, or corrective footwear other causes of foot pain such as Achilles tendonitis, hallux valgus and ankle sprain \-

Design outcomes

Primary

MeasureTime frameDescription
Foot Pain4 weeksFoot pain measured via Visual Analogue Scale (0 to 100 mm), in which low score signifies less pain and higher score signifies more pain.
Functional Ability4 weeksFunctional Ability will be measured using Foot Function Index (FDI) which is a self-administered questionnaire (23 items), and a lower score signifies less functional disability whereas a higher score signifies higher functional disability
Gait Velocity4 weeksHigher gait velocity signifies better outcome
Stride Length4 weeksA higher stride length signifies better functional outcome
Cadence4 weeksA higher cadence signifies a better functional outcome

Countries

Pakistan

Contacts

PRINCIPAL_INVESTIGATORIrsa Aftab, DPT

IIUI

STUDY_CHAIRMuhammad Osama, PhD

IIUI

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 30, 2026