Patellar Tendon Physiotheraphy Acute Effects Trial (PTPAFT)

January 5, 2026 updated by: Elif Akduran, Dokuz Eylul University

Investigation of the Acute Effects of Different Physiotherapy Methods Applied to the Patellar Tendon: A Single-Blind Randomized Controlled Trial

This randomized controlled trial investigated the acute effects of different physiotherapy interventions applied to the patellar tendon. Participants were randomly assigned to one of four groups: deep friction massage, thermal agent application, quadriceps resistance exercise, or a control group. Each intervention was delivered in a single session. Outcomes of the study included changes in skin temperature, muscle strength, flexibility, and pulse rate. All measurements were taken immediately before the intervention and again immediately after, 15 minutes after, and 60 minutes after the intervention. The study was conducted with healthy adult volunteers. The results of this study are expected to contribute to a better understanding of how different physiotherapy modalities acutely influence the patellar tendon region.

Study Overview

Detailed Description

This study examined the immediate physiological responses of the patellar tendon region following different physiotherapy interventions. Participants were allocated into four groups: (1) deep friction massage applied directly to the patellar tendon, (2) a locally applied superficial thermal agent, (3) a structured quadriceps resistance exercise protocol, and (4) a no-intervention control group. Each intervention was administered as a single session under standardized laboratory conditions.

Outcome measures included skin temperature assessed with thermal imaging, quadriceps muscle strength measured with a handheld dynamometer, flexibility assessed by standardized clinical procedures, and pulse rate. All measurements were collected at four time points: immediately before the intervention, immediately after, 15 minutes after, and 60 minutes after the intervention.

The study was conducted with healthy adult volunteers to evaluate the acute physiological effects of commonly used physiotherapy modalities on the patellar tendon region. The findings are intended to inform clinical decision-making by clarifying how different physiotherapy techniques influence tendon-related parameters within the first hour following treatment.

Study Type

Interventional

Enrollment (Actual)

84

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • balçova
      • Izmir, balçova, Turkey (Türkiye), 35330
        • Dokuz Eylül University, İzmir

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Ages 18 to 24 years
  • Not having engaged in regular exercise training within the past 6 months
  • Body Mass Index (BMI) below 30
  • Ability to complete all assessment procedures
  • Ability to understand the study procedures and provide written informed consent

Exclusion Criteria:

  • Presence of any systemic or musculoskeletal disorder
  • Onset of pain during the assessment procedure
  • History of knee joint or peri-articular injury within the past 6 months
  • Presence of neurological, vascular, or rheumatological disease
  • Any dermatological condition that may affect skin integrity

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Deep Friction Massage
A single session of deep friction massage applied directly to the patellar tendon
A single session of deep friction massage applied directly to the patellar tendon.
Experimental: Thermal Agent Application
A locally applied superficial thermal agent delivered as a single session.
A single application of a thermal agent (hot pack) applied to the patellar tendon region.
Experimental: Quadriceps Exercise
A single session of standardized quadriceps resistance exercise protocol.
A single session of quadriceps resistance exercise targeting knee extensor muscles.
No Intervention: Control
No treatment administered; participants remained at rest during the session.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Skin Temperature Change
Time Frame: Baseline, immediately after intervention, 15 minutes after, 60 minutes after
Skin temperature of the patellar tendon region measured using infrared thermography at four time points to analyze acute thermal response.
Baseline, immediately after intervention, 15 minutes after, 60 minutes after
Quadirceps Muscle Strength
Time Frame: Baseline, immediately after intervention, 15 minutes after, 60 minutes after
Isometric quadriceps muscle strength measured with a handheld dynamometer at four time points to assess acute changes following intervention.
Baseline, immediately after intervention, 15 minutes after, 60 minutes after
Hamstring and Quadriceps Flexibility
Time Frame: Baseline, immediately after intervention, 15 minutes after, 60 minutes after
Flexibility of the quadriceps and hamstring assessed using a standardized stretching test at four time points to assess evaluate changes.
Baseline, immediately after intervention, 15 minutes after, 60 minutes after
Dorsalis Pedis Pulse Rate
Time Frame: Baseline, immediately after intervention, 15 minutes after, 60 minutes after
Pulse rate measured by palpation at four time points (baseline, immediately after intervention, 15 minutes, and 60 minutes) to evaluate acute cardiovascular response to the intervention.
Baseline, immediately after intervention, 15 minutes after, 60 minutes after

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 25, 2025

Primary Completion (Actual)

June 20, 2025

Study Completion (Actual)

December 1, 2025

Study Registration Dates

First Submitted

December 21, 2025

First Submitted That Met QC Criteria

December 21, 2025

First Posted (Estimated)

January 5, 2026

Study Record Updates

Last Update Posted (Actual)

January 7, 2026

Last Update Submitted That Met QC Criteria

January 5, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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