NCT07695064

Brief Summary

This was a randomized controlled trial done to to compare the effect of manual Cross Friction Massage and IASTM in reducing pain , range of motion and functional disability in patients with chronic lateral epicondylitis

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 11, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 28, 2026

Completed
4 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 2, 2026

Completed
4 days until next milestone

First Submitted

Initial submission to the registry

July 6, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 10, 2026

Completed
Last Updated

July 10, 2026

Status Verified

July 1, 2026

Enrollment Period

6 months

First QC Date

July 6, 2026

Last Update Submit

July 6, 2026

Conditions

Outcome Measures

Primary Outcomes (3)

  • Visual Analog Scale.

    A Visual Analogue Scale (VAS) was used to measure pain intensity during rest. The level of pain was recorded on a 10 cm line where 0 was classified as "no pain" and 10 was classified as "worst possible pain". Subjects were asked to indicate their pain level by placing a mark along this horizontal line

    Assessments were performed at baseline (week 0) and post intervention (week 6).

  • Goniometer

    ROM measured was used a standard universal goniometer, which is considered a valid, reliable, and widely accepted clinical tool for assessing joint angles in musculoskeletal conditions. Measurements were taken for wrist flexion, wrist extension, and elbow movements, following standardized positioning and landmark alignment to ensure consistency and accuracy.

    Assessments was performed at baseline (week 0) and post intervention (week 6).

  • Patient-Rated Tennis Elbow Evaluation (PRTEE) questionnaire

    Patient-Rated Tennis Elbow Evaluation (PRTEE) questionnaire The Patient-Rated Tennis Elbow Evaluation (PRTEE) questionnaire is an instrument that has been developed specifically for use with this disorder \[16\]. It takes the form of a 15-item questionnaire, with five items addressing pain and 10 concerned with functional deficit. For each item, the respondent uses a 0- 10 numerical scale to rate the average pain or difficulty they have experienced over the previous week while carrying out various activities that are commonly painful in tennis elbow. The marking system ensures that pain and function are weighted equally in the total score. Higher scores represent greater se- verity and the maximum score is 100

    Assessments was performed at baseline (week 0) and post intervention (week 6).

Study Arms (2)

Manual Cross Friction Massage (CFM)

EXPERIMENTAL

Arm Description: Patient seated , elbow flexed \~90 degree , forearm pronated , extensor tendon exposed and released. Thumb / index finger applies firm transverse pressure .

Other: Manual Cross Friction Massage (CFM)

Group B: Instrument-Assisted Soft Tissue Mobilization (IASTM)

ACTIVE COMPARATOR

Seated,Elbow flexed \~ 90 degree , forearm pronated, extensor tendon exposed and relaxed. Stainless steel IASTMCurve bar S shape , dual grip tool was used with moderate ,tolerable pressure .

Other: Instrument-Assisted Soft Tissue Mobilization (IASTM)

Interventions

Patient seated , elbow flexed \~90 degree , forearm pronated , extensor tendon exposed and released. Thumb / index finger applies firm transverse pressure . Short , deep ,rhythmic strokes perpendicular to ECRB tendon fibers (5 to 10 min ).Total duration 35 - 40 mins. 3 sessions per week for 6 weeks.

Manual Cross Friction Massage (CFM)

Seated,Elbow flexed \~ 90 degree , forearm pronated, extensor tendon exposed and relaxed. Stainless steel IASTMCurve bar S shape , dual grip tool was used with moderate ,tolerable pressure . Longitudinal sweeping (1-2 min ) , Cross fiber stokes (1-2 min), Fanning over tender point ( 1- 2min). Flushing stokes (1min).40 -45 mins total time . 3 sessions per week for 6 weeks.

Group B: Instrument-Assisted Soft Tissue Mobilization (IASTM)

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Both male and female aged between 18 to 60 years with a clinical diagnosis of lateral elbow pain lasting for≥ 6 months duration VAS score ≥ 4 during resisted wrist extension or grip activity ≥1 of the following tests being positive . Mill's test pain on passive wrist flexion and elbow extension Cozen's test pain on resisted wrist extension, elbow extended, wrist in flexion and medial deviation .
  • Painful palpation at the origin of the ECRB or lateral epicondyle

You may not qualify if:

  • Participants will be excluded as:
  • History of recent fracture,dislocation,or surgery near the elbow joint in the last 3 month Neurological or systemic inflammatory conditions (e.g., rheumatoid arthritis) Current use of corticosteroid injections in the elbow region within the past 6 weeks Previous physiotherapy interventions for the same complaint in the last 3 months.
  • Skin disorders or open wounds near the treatment area.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ibadat International University, Islamabad

Peshawar, KPK, 25000, Pakistan

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Group A : Manual Cross Friction Massage (CFM) Group B: Instrument-Assisted Soft Tissue Mobilization (IASTM)
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 6, 2026

First Posted

July 10, 2026

Study Start

January 11, 2026

Primary Completion

June 28, 2026

Study Completion

July 2, 2026

Last Updated

July 10, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share

Locations