- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07315906
Patellar Tendon Physiotheraphy Acute Effects Trial (PTPAFT)
Investigation of the Acute Effects of Different Physiotherapy Methods Applied to the Patellar Tendon: A Single-Blind Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
balçova
-
Izmir, balçova, Turkey (Türkiye), 35330
- Dokuz Eylül University, İzmir
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PTT-2025-DEU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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