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Clinical Trials in Spain / NCT07842926
Recruiting Not applicable

Acute Effects of Capacitive-Resistive Radiofrequency Therapy in People With Parkinson's Disease

NCT07842926 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-09-21
Last updated
2026-09-25

Condition(s) studied

Parkinson Disease (PD)

Investigational drug(s) / intervention(s)

Capacitive Radiofrequency TherapyResistive Radiofrequency TherapyCapacitive-Resistive Radiofrequency TherapyResistive-Capacitive Radiofrequency Therapy

Capacitive Radiofrequency Therapy: Capacitive-resistive radiofrequency therapy (TECAR) will be applied in capacitive mode to the lower limbs for 15 minutes per leg. Treatment will target the posterior lower leg, quadriceps, and hamstring muscle regions. Intensity will be individually adjusted to a medium-high level producing a clear but comfortable thermal effect, approximately 3-4 out of 5 on the device intensity scale.

Resistive Radiofrequency Therapy: Capacitive-resistive radiofrequency therapy (TECAR) will be applied in resistive mode to the lower limbs for 15 minutes per leg. Treatment will target the posterior lower leg, quadriceps, and hamstring muscle regions. Intensity will be individually adjusted to a medium-high level producing a clear but comfortable thermal effect, approximately 3-4 out of 5 on the device intensity scale.

Capacitive-Resistive Radiofrequency Therapy: Capacitive-resistive radiofrequency therapy (TECAR) will be applied to the lower limbs using a mixed protocol consisting of 10 minutes of capacitive treatment followed by 5 minutes of resistive treatment per leg. Treatment will target the posterior lower leg, quadriceps, and hamstring muscle regions. Intensity will be individually adjusted to a medium-high level producing a clear but comfortable thermal effect, approximately 3-4 out of 5 on the device intensity scale.

Resistive-Capacitive Radiofrequency Therapy: Capacitive-resistive radiofrequency therapy (TECAR) will be applied to the lower limbs using a mixed protocol consisting of 10 minutes of resistive treatment followed by 5 minutes of capacitive treatment per leg. Treatment will target the posterior lower leg, quadriceps, and hamstring muscle regions. Intensity will be individually adjusted to a medium-high level producing a clear but comfortable thermal effect, approximately 3-4 out of 5 on the device intensity scale.

Study summary

This study will investigate the immediate and short-term effects of capacitive-resistive radiofrequency therapy (TECAR) applied to the lower limbs in people with Parkinson's disease. The main aim is to determine which of four different TECAR application protocols produces the greatest improvement in muscle stiffness and walking function.

Twenty participants with Parkinson's disease will receive four different TECAR protocols in four separate sessions. The protocols will include capacitive treatment, resistive treatment, and two combinations of capacitive and resistive treatment. Each participant will receive all four protocols, and the order in which they are applied will be randomized. Sessions will be separated by a 7-day washout period.

Muscle stiffness will be measured using the MyotonPRO device. Walking and functional mobility will also be assessed using the Timed Up and Go test and the 10-Metre Walk Test. Joint range of motion and lower-limb musculoskeletal pain will also be evaluated. Measurements will be performed immediately before treatment, immediately after treatment, and 48 hours after each session.

The study will also record any discomfort or adverse events associated with TECAR therapy to evaluate the safety and tolerability of the different treatment protocols.

Eligibility

Sex
ALL
Min age
55 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 55 and 90 years. Clinical diagnosis of idiopathic Parkinson's disease confirmed by a Neurology specialist. Hoehn and Yahr stage II or III. Functional walking ability. Clinically relevant lower-limb rigidity in at least one leg, defined as a score ≥2 on item 3.3d (right lower limb) or 3.3e (left lower limb) of Part III of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS). Stable antiparkinsonian pharmacological treatment during the previous 4 weeks, with no planned changes during the intervention period. Ability to understand and follow simple instructions, defined as a score \>24 on the validated Spanish version of the Mini-Mental State Examination (MMSE-MEC). Provision of written informed consent. Exclusion Criteria: * Advanced Parkinson's disease, defined as Hoehn and Yahr stage \>III, with severe postural instability. Other neurological or musculoskeletal conditions that could interfere with the assessment of lower-limb rigidity or gait. Skin lesions, open wounds, or infection in the area where radiofrequency therapy will be applied. Presence of a pacemaker, defibrillator, other implanted electronic device, or another contraindication to TECAR therapy, such as altered thermal sensitivity. Lower-limb surgery within the previous 6 months.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Asociación Parkinson Aragón Zaragoza Zaragoza Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07842926 on ClinicalTrials.gov ↗ ← All trials in Spain