Skip to content

COMPARATIVE EFFECTS OF INSTRUMENT ASSISTED SOFT TISSUE MOBILIZATION AND DEEP TRANSVERSE FRICTION MASSAGE ON SUBJECTS WITH ACHILLES TENDINOPATHY

COMPARATIVE EFFECTS OF INSTRUMENT ASSISTED SOFT TISSUE MOBILIZATION AND DEEP TRANSVERSE FRICTION MASSAGE ON SUBJECTS WITH ACHILLES TENDINOPATHY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240429061592N1
Enrollment
40
Registered
2024-05-10
Start date
2024-02-17
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Achilles Tendinopathy. Achilles Tendinopathy

Interventions

Intervention group:.

Sponsors

THE UNIVERSITY OF FAISALABAD
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 18 to 40 years of age Clinically diagnosed with AT by a clinician Pain that is localized 2-7 cm from the tendon's distal insertion Patient with U/L or B/L AT Having pain greater than 3 on NPRS Positive Royal London hospital test Positive Arc sign Willing to participate will be included into study

Exclusion criteria

Exclusion criteria: Past history of ankle fracture that affect joint Having pain 3 or less than 3 on NPRS Insertional tendinopathy Rheumatic conditions Diabetes or circulatory issues Achilles tendon injuries other than AT Positive Thompson’s test Patient with age less than 18 years or above than 40 years Participants with any diagnosed auto-immune disorder Having co-morbidities such as neoplasm

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before Intervention and at the end of 3rd week. Method of measurement: NPRS.

Secondary

MeasureTime frame
Functional Disability. Timepoint: Before Intervention and after 3rd week. Method of measurement: VISA-A Achilles Questionnaire.

Countries

Pakistan

Contacts

Public ContactSameer Ul Haq

Al Haq Physio & Rehablition Center

sameerulhaq076@gmail.com+92 342 0817195

Outcome results

None listed

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