NCT07797764

Brief Summary

Patellar tendinopathy (PT) is a commonly used term for the clinical manifestation of patellar tendon pain and functional limitation with multifactorial etiology. It occurs in both athletes and general population in all age groups. It is often characterized as an overuse injury resulting from chronic failure of the healing response that is not strictly linked to inflammatory or degenerative processes.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Aug 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress49%
Aug 2026Nov 2026

Study Start

First participant enrolled

August 20, 2026

Completed
7 days until next milestone

First Submitted

Initial submission to the registry

August 27, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 1, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 20, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 20, 2026

Last Updated

September 1, 2026

Status Verified

August 1, 2026

Enrollment Period

2 months

First QC Date

August 27, 2026

Last Update Submit

August 27, 2026

Conditions

Keywords

Patellar tendinopathyKinesiophobiaShock wave therapySensorimotor function

Outcome Measures

Primary Outcomes (5)

  • Digital inclinometer

    4 months

  • Tampa scale for Kinesiophobia

    4 months

  • Biodex balance system (overall stability index)

    4 months

  • Biodex balance system (Anteroposterior)

    4 months

  • Biodex balance system (Mediolateral)

    4 months

Study Arms (1)

Study group

EXPERIMENTAL
Device: Extracorporeal Shockwave Therapy

Interventions

The low-energy focused ESWT was applied using the BTL-6000 FSWT device with piezoelectric generator and a coupling pad which modulates penetration depth to 0-35 mm. The setting was chosen based on ISMST guidelines (https://shockwavether apy.org). Energy flux density varied between 0.14 and 0.18 mJ/ mm2 due to patient tolerance, frequency was set at 8 Hz. A total of 2000 shocks were applied semi-statically to the most defined pathological area in the patellar tendon followed by2000 shocks dynamically to the quadriceps muscle.

Study group

Eligibility Criteria

Age15 Years - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Has patellar tendon pain, which limits (at least in part) the quality of normal daily.
  • Has clinical manifestation of PT (pain and impaired function) confirmed by a clinician.
  • Has symptoms only in one leg, the other one is asymptomatic.
  • Normal BMI.

You may not qualify if:

  • Any contraindication for ESWT is present (according to the International Society for Medical Shockwave Treatment \[ISMST\] consensus at https://shockwavetherapy.org).
  • They were aware of any symptomatic mechanical tendon damage in the past (e.g. partial or complete rupture in relation to the injury), neurological, oncological, or systemic disease (e.g. neuropathy, lupus or rheumatic arthritis) coexists
  • They were already treated for PT elsewhere up to 3 months prior to the study (e.g. platelet- rich plasma therapy, physiotherapy incl. resistance training or ESWT).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Al Ryada University for Science and Technology

Sadat, Menoufia, Egypt

Location

MeSH Terms

Conditions

Kinesiophobia

Interventions

Extracorporeal Shockwave Therapy

Condition Hierarchy (Ancestors)

Phobic DisordersAnxiety DisordersMental Disorders

Intervention Hierarchy (Ancestors)

Ultrasonic TherapyDiathermyHyperthermia, InducedTherapeuticsPhysical Therapy ModalitiesRehabilitation

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Lecturer of Physical Therapy for Neurology and its Surgery Faculty of Physical Therapy - Al Ryada University for Science and Technology

Study Record Dates

First Submitted

August 27, 2026

First Posted

September 1, 2026

Study Start

August 20, 2026

Primary Completion (Estimated)

October 20, 2026

Study Completion (Estimated)

November 20, 2026

Last Updated

September 1, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations