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NCT06392802Completed

Effectiveness of a Rehabilitation Exercise Plan at Home to Treat Post-stroke Patients in the Chronic Phase

Source: ClinicalTrials.gov · Last updated 3 Sept 2026

Brief summary (registry, in English)

Background: Stroke is the second leading cause of death worldwide and the primary medical cause of disability. It is estimated that 45% of affected individuals will continue to have moderate or severe functional disabilities throughout their lives. According to the American Stroke Association, telerehabilitation has the potential to provide timely and efficient care to stroke survivors, improving patients' functional outcomes while reducing long-term disability and associated costs. Hypothesis: Through the developed application (Muvity), the study aims to contribute to the validity of telerehabilitation and virtual reality as beneficial tools for rehabilitation, specifically for individuals in the post-stroke sequelae phase. Objectives: To evaluate the effectiveness of a non-immersive virtual reality program in telerehabilitation for patients who have experienced a stroke more than 6 months ago. Methodology: Prospective longitudinal study with single blinding. The control group undergoes a conventional intervention, while the experimental group undergoes an innovative intervention (n=25). Variables: The collected variables and measurement tools include upper extremity functionality (Fugl-Meyer scale), balance (Berg), functional independence (Barthel), pain (Brief Pain Inventory), post-stroke quality of life (ECVI-38), emotional health (UCLA Self-Rating Depression Scale), treatment expectations (Expectation for Treatment Scale), treatment adherence (through an APP), and satisfaction (Telehealth Usability Questionnaire). Statistical Analysis: Data will be analyzed per protocol (PP); the normality distribution of the data will be assessed, and results will be analyzed using parametric or non-parametric techniques depending on normality. A bivariate analysis will compare results between the control and intervention groups, considering a statistically significant result when p \< 0.05. Expected Results: Similar results are expected between groups or slightly favorable outcomes in the experimental group for the different variables. Applicability and Relevance: The application would facilitate access to motor rehabilitation treatments in an enjoyable and engaging manner, promoting physical activity and contributing to a healthy lifestyle. Upon obtaining the results of this study, a trial implementation of the application in five socio-sanitary or associative centers is planned to verify its final applicability.

Status (registry)
Completed
Study type
Interventional
Enrollment
39 (actual)
First submitted
17 Jan 2024
Start date
1 Mar 2023
Primary completion date
28 Feb 2025
Lead sponsor
Universitat Politècnica de Catalunya
Diseases
Stroke
NCT number
NCT06392802

What you commit to

  • Study type: Interventional
  • Participants enrolled: 39
  • From 1 Mar 2023 to the primary completion date, 28 Feb 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Engaging in intense physical therapies.

Other

  • Severe aphasia: inability or difficulty communicating through speech.
  • Cognitive impairments affecting short and mid-term memory.
  • Vision: having visual deficits in either eye that may impair screen visualization.
  • Vision: experiencing hemispatial neglect, meaning difficulty processing stimuli on the side opposite to the injury.

Who the study is looking for

  • Age: between 18 and 85 years old.
  • Stroke duration of more than six months + Discharge from post-stroke rehabilitation.
  • Moderate physical disability: scoring between 1-3 on the Modified Rankin Scale.
  • Standing: able to stand safely for 2 minutes without support (maximum score -4- on item 2 of the Berg Scale).
  • Vision: capable of correctly visualizing a screen at a distance of 2 meters.
  • Cognitive status: No cognitive impairment or mild cognitive impairment (Mini-Mental State Examination score ≥ 24). Ability to understand and follow verbal instructions in Catalan or Spanish.
  • Technological skills: capable of basic use of a mobile phone and computer (keyboard, mouse, screen).
  • Glenohumeral joint mobility: minimum of 30º flexion, abduction, horizontal abduction; and 15º internal and external rotation.
  • Elbow joint mobility: minimum of 45º flexion.

Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitat Politècnica de Catalunya
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status
Associació Disminuïts Físics d'Osona
Coordinator of this site? Confirm its status
VicSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.