Clinical trials

6

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effects of Transcutaneous Vagus Nerve Stimulation in Parkinson´s Disease

This study aims to determine whether electrical stimulation of the ear, when combined with physical and speech therapy, can improve symptoms in subjects diagnosed with Parkinson´s disease, by comparing two different application sites. Each subject will undergo an initial in-person screening and provide consent before participating in the study. The main questions to answer are: * Does transcutaneous electrical nerve stimulation (tVNS) in the ear paired with physical and speech therapy improve speech and voice-related problems, airway protection, salivation, and swallowing? * Does tVNS paired with physical and speech therapy improve tremor, walking speed, and balance in people with PD? * Does tVNS paired with physical and speech therapy improve heart rate and heart rate variability in people with PD? * Do its effects persist at 8 weeks? Participants will: Attend 12 rehabilitation sessions over 4 weeks (three per week). During each session, participants received either active or sham tVNS, accompanied by speech therapy (once per week), physical therapy (once per week), or conducted alone (once per week). Undergo speech, voice, swallowing, respiratory, gait, balance, tremor, heart rate variability, and cognitive testing, as well as questionnaires regarding the quality of life, before and after treatment. Return for a follow-up visit eight weeks after therapy to check how long the effects last.

Participants needed: 46
Trial details
Biological sex: AllType: InterventionalSponsor: Universidade da CoruñaUpdated: May 19, 2026Locations: 1
Eligibility criteria

Being a member of the Association or be interested in joining; [+4]

Any contraindication for taVNS (e.g., ear lesions, pacemakers, defibrillators, o... [+7]

Status: Recruiting

Cardiometabolic Adaptations to Concurrent Training: Effect of Effort Configuration on Postmenopausal Women

The main objectives of this project are to assess the effects of a 20-week concurrent training program on neuromuscular adaptations, body composition, cardiometabolic health, quality of life, mood state, physical self-perception, and menopause-related symptoms in physically active postmenopausal women, and to compare the adaptations resulting from different combinations of endurance and resistance training programs with varying effort configurations. Additionally, this project aims to examine the longitudinal interaction and potential interference effects between endurance and resistance training effort configurations throughout the training program and to determine the optimal combination of effort configurations that maximizes health benefits in concurrent training programs for physically active postmenopausal women.

Participants needed: 60
Trial details
Age: 46-65Biological sex: FemaleType: InterventionalSponsor: Universidade da CoruñaUpdated: Apr 28, 2026Locations: 1
Eligibility criteria

At least one year since the last menstrual period. [+4]

Diagnosis of grade 2 or grade 3 hypertension. [+3]

Status: Not yet recruiting

Acute Cardiovascular and Neuromuscular Responses to Walking With Blood Flow Restriction (BFR) in Older Adults

The goal of this clinical trial is to explore how walking combined with different levels of partial blood flow restriction (BFR) affects cardiovascular, neuromuscular, and movement (kinematic) variables in older adults. The main questions it aims to answer are: Does walking with BFR increase internal effort, as shown by cardiovascular changes, and is this effect proportional to the level of restriction? Does walking with BFR temporarily reduce neuromuscular control, and is this reduction greater at higher restriction levels? Does walking with BFR change gait movement patterns? This study uses a crossover design, meaning that each participant will complete all four conditions and serve as their own control. Participants will: Take part in walking sessions under four conditions with different levels of restriction: BFR40%, BFR80%, SHAM (0% BFR), and CON (without BFR). Have their cardiovascular responses, muscle performance, and gait movement patterns measured. Report their perceptions of the sessions, including Rate of Perceived Exertion (RPE), satisfaction, and possible side effects.

Participants needed: 20
Trial details
Age: 60-90Biological sex: AllType: InterventionalSponsor: Universidade da CoruñaUpdated: Dec 10, 2025Locations: 2
Eligibility criteria

Being institutionalized. [+3]

Status: Not yet recruiting

Exercise and Physical Activity in Adults with Acquired Brain Injury

Exercise and physical activity in adults with acquired brain injury

Participants needed: 30
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: Universidade da CoruñaUpdated: Mar 26, 2025
Eligibility criteria

Aged more than 18 years of age and present a medical diagnosis of acquired brain... [+2]

Have medical comorbidities that contraindicate the safe performance of the progr... [+1]

Status: Not yet recruiting

Knee Osteoarthritis, Motor Control, Risk of Falls and Virtual Reality

The goal of this clinical trial is to learn about knee osteoarthritis, functionality, and risk of falls in community-dwelling adults aged 60 years and older. The main questions it aims to answer are: * What are the characteristics of a community-dwelling population over 60 years and older in terms of knee osteoarthritis, functionality, and risk of falls? * Does an intervention with virtual reality lower knee osteoarthritis symptoms, raise functionality and prevent falls in community-dwelling adults aged 60 years and older, compared to a control group receiving conventional physiotherapy treatment based on therapeutic exercise? Participants will: * Answer questionnaires. * Perform physical laboratory tests through a camera-based motion capture system. * Execute task-based exercises in a virtual environment through virtual reality. Researchers will compare community-dwelling adults aged 60 years and older who execute task based exercises in a virtual environment through virtual reality and community-dwelling adults aged 60 years and older receiving conventional physiotherapy treatment based on therapeutic exercise to see if virtual reality improves knee osteoarthritis symptoms, functionality, and lowers fall risk.

Participants needed: 110
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Universidade da CoruñaUpdated: Mar 17, 2025
Eligibility criteria

Age over 60 years. [+5]

History of significant previous traumas or surgeries to the spine, pelvis, or le... [+6]

Status: Recruiting

Wereables for Upper Limb Functionality in Hemiparesis

The project is configured as a national interventional study that aims to determine the effectiveness of an intervention strategy using wearable technology, tailored to improve function (WeFun-wearable), on the spontaneous use of the affected upper extremity, activities of daily living and the participation in children with unilateral cerebral palsy.

Participants needed: 40
Trial details
Phase: Phase 2, Phase 3Age: 3-8Biological sex: AllType: InterventionalSponsor: Universidade da CoruñaUpdated: Mar 12, 2025Locations: 1
Eligibility criteria

Confirmed diagnosis of UCP. [+2]

Botulinum toxin injection or surgical interventions in the upper limb within 6 m... [+7]