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Unlocking the Hidden Effects of Shockwave: Longitudinal Changes in Sensorimotor Function and Kinesiophobia in Adolescents With Patellar Tendinopathy

Unlocking the Hidden Effects of Shockwave: Longitudinal Changes in Sensorimotor Function and Kinesiophobia in Adolescents With Patellar Tendinopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07797764
Enrollment
50
Registered
2026-09-01
Start date
2026-08-20
Completion date
2026-11-20
Last updated
2026-09-01

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

Conditions

Patellar Tendinopathy

Keywords

Patellar tendinopathy, Kinesiophobia, Shock wave therapy, Sensorimotor function

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.

Detailed description

Once enrolled, participants were examined by a physiotherapist, and received the first application of ESWT (week 0). At weekly intervals, they received three more applications and on the day of the last application (week 3), a control clinical examination was performed. In the 12th-week follow-up after the last application week 15), a final examination including joint position sense, balance and kinesiophobia evaluation was performed.

Interventions

DEVICEExtracorporeal Shockwave Therapy

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.

Sponsors

Ahmed Alshimy
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* 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).

Design outcomes

Primary

MeasureTime frame
Digital inclinometer4 months
Tampa scale for Kinesiophobia4 months
Biodex balance system (overall stability index)4 months
Biodex balance system (Anteroposterior)4 months
Biodex balance system (Mediolateral)4 months

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 2, 2026