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To verify the feasibility and effectiveness of a distance Rehabilitation Program in the treatment of patients with Parkinson's Disease

Clinical trial to verify the feasibility and effectiveness of a Mixed Remote Individual Rehabilitation Program in the treatment of patients with Parkinson's Disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6sz837s
Enrollment
Unknown
Registered
2022-10-30
Start date
2021-05-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Parkinson's Disease

Interventions

This is a two-arm, single-blind, randomized controlled clinical study. Intervention group: 10 people with Parkinson's disease, men and women, will be seen by the physical therapist 3 times a week thro

Sponsors

Bruno Lopes dos Santos Lobato
Lead Sponsor
Universidade Federal do Pará
Collaborator

Eligibility

Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed with idiopathic Parkinson's disease according to the London Brain Bank diagnostic criteria; Age between 30 and 80 years; Mild stage disease (Hoehn and Yahr equal to or less than 2); Use of pharmacological dopaminergic treatment at a stable dose for at least one month, with the possibility of remaining unchanged during the intervention period

Exclusion criteria

Exclusion criteria: Any type of atypical secondary parkinsonism; Treatment with any drug or experimental intervention in the last 90 days; Presence of severe psychotic symptoms (score greater than 2 in item 1.2 of the International Parkinson and Movement Disorders Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS); Diagnosis of dementia determined by the flowchart proposed by the Movement Disorders Society; Presence of severe systemic diseases or decompensated such as: infections, severe heart disease, malignant neoplasm, liver or kidney failure, poorly controlled diabetes; Presence of orthopedic diseases, other neurological diseases or cardiac comorbidities that prevent or pose a risk for performing aerobic or stretching exercises; Patients without access to internet at home; Patients who are unable to perform tasks on the computer, or without family assistance needed for remote activities

Design outcomes

Primary

MeasureTime frame
Evaluate patients' adherence to interventions and the occurrence of adverse effects, such as safety measures, at the end of the fourth week of treatment in relation to the baseline evaluation

Secondary

MeasureTime frame
Improvements are expected in the scores of the International Parkinson and Movement Disorders Society- Unified Parkinson's Disease Rating Scale (MDS-UPDRS) and in the Hoehn and Yahr Staging (HY), a scale used to measure the severity of Parkinson's disease.;Assessment of gait and balance, through the Time Up and Go instrumented test.;It is expected to find improvement in the assessment scale of confidence in balance, 5 times Sit and Stand test, 6-minute walk test to assess physical capacity;;It is expected to see an improvement in the Montreal Cognitive Assessment (MoCA) for cognitive screening, a 15-item Geriatric Depression Scale for brief screening for the presence of depression, a scale that scores the response to interventions- Clinician's Global Impression of Change (CGI-C) , and in the questionnaire composed of 8 questions that assess aspects of the patient's quality of life - Parkinson's Disease Questionnaire (PDQ-8).

Countries

Brazil

Contacts

Public ContactTamires Vilacorta Pereira

Universidade Federal do Pará

tamires.pereira@npo.ufpa.br55(91)983217743

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 8, 2026