Telerehabilitation Using a Dance Intervention in People With Parkinson's Disease
5 april 2021 uppdaterad av: Aline de Souza Pagnussat, Federal University of Health Science of Porto Alegre
The aim of this study is to verify the feasibility of a telerehabilitation approach with dance in people with parkinson's disease.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This is a feasibility study that aims to investigate the safety and efficacy of dance classes via an online platform in people with and without Parkinson's Disease.
The intervention will last 2 months and the classes will be conducted twice a week (60 minutes) using the Zoom platform.
Evaluations will be performed before and after the intervention by means of the Zoom platform as well and will include questionnaires of quality of life, depression, anxiety, and activities of daily living.
Studietyp
Interventionell
Inskrivning (Faktisk)
24
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Rio Grande Do Sul
-
Porto Alegre, Rio Grande Do Sul, Brasilien, 90050-170
- Universidade Federal de Ciências da Saúde de Porto Alegre
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
45 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Individuals with and without parkinson's disease according London Brain Bank Criteria
- Minimal cognitive ability to understand commands (MMSE)
- Able to stand at least 10 minutes with or without support
- Dopamine medication stable at least 6 weeks before the beginning of the study
- Portable device and internet connection
Exclusion Criteria:
- Severe visual or auditive disturbances
- Neurological disease (other than parkinson's for those included) or severe neuromuscular disorders that prejudice the proposed activities
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: telerehabilitation with dance (Parkinson's)
This group will receive dance classes online during 60 minutes, twice a week for 8 weeks.
|
Dance classes will be provided through a online platform.
Each class will last 60 minutes, twice a week, during 8 weeks.
|
|
Aktiv komparator: telerehabilitation with dance (Healthy controls)
This group will receive dance classes online during 60 minutes, twice a week for 8 weeks.
|
Dance classes will be provided through a online platform.
Each class will last 60 minutes, twice a week, during 8 weeks.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
feasibility (adherence rates)
Tidsram: 10 weeks
|
To assess the feasibility of the study design and procedures.
The adherence rate will be calculated by the total number of patients who completed the full course of intervention divided by the total number of patients included at the beginning.
|
10 weeks
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
feasibility (patients opinions)
Tidsram: 10 weeks
|
Semi structured interviews will involve gaining patients opinions on the strengths and weaknesses of the intervention
|
10 weeks
|
|
feasibility (safety and usability)
Tidsram: 10 weeks
|
The researches will follow all patients during the intervention regarding safety (i.e.
falls) and usability (i.e.
internet connection)
|
10 weeks
|
|
Parkinson's Disease Questionnaire-8 (PDQ-8)
Tidsram: Change from Pre to Post treatment (10 weeks)
|
The PDQ-8 is a short-form version to assess quality of life in persons with Parkinson's disease.
Each question is scored from 0-4 points and the scores are summed and given as a percentage score (0-100).
The higher the score, the worse the patient's condition.
|
Change from Pre to Post treatment (10 weeks)
|
|
36-Item Short Form Survey (SF-36)
Tidsram: Change from Pre to Post treatment (10 weeks)
|
The SF-36 measures health-related quality of life.
This questionnaire has 36-item measure divided into 8 subscales - each subscale can be used independently.
Each of the 8 summed scores is transformed into a scale from 0 (negative health) to 100 (positive health)
|
Change from Pre to Post treatment (10 weeks)
|
|
Hospital Anxiety and Depression Scale (HADS)
Tidsram: Change from Pre to Post treatment (10 weeks)
|
The scale is used to identify depression and anxiety and presents 14 items.
The total score is out of 42.
The higher scores indicate greater levels of anxiety and depression.
|
Change from Pre to Post treatment (10 weeks)
|
|
Unified Parkinson's Disease Rating Scale (UPDRS) Part I
Tidsram: Change from Pre to Post treatment (10 weeks)
|
The Part I concerns about non-motor experiences of daily living (e.g.
anxiety and depression).
This scale has 13 questions and all items have 5 response options.
Higher scores indicate greater impact of PD symptoms.
|
Change from Pre to Post treatment (10 weeks)
|
|
Activities-Specific Balance (ABC) Scale
Tidsram: Change from Pre to Post treatment (10 weeks)
|
Self-reported questionnaire measuring self-efficacy in performing activities without losing balance.
The ABC Scale consists of 16 questions that require the patient to rate their confidence on a scale from 0% to 100%.
The higher the percentage, the higher level of physical functioning.
|
Change from Pre to Post treatment (10 weeks)
|
|
Five Times Sit to Stand Test (FTSTS)
Tidsram: Change from Pre to Post treatment (10 weeks)
|
The test assess the functional mobility strength of lower extremity (measured by the time to complete the test).
The higher the time to complete the test, the lower the performance.
|
Change from Pre to Post treatment (10 weeks)
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
5 september 2020
Primärt slutförande (Faktisk)
5 oktober 2020
Avslutad studie (Faktisk)
5 december 2020
Studieregistreringsdatum
Först inskickad
1 oktober 2020
Först inskickad som uppfyllde QC-kriterierna
7 oktober 2020
Första postat (Faktisk)
9 oktober 2020
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
6 april 2021
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
5 april 2021
Senast verifierad
1 april 2021
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- TELEDANCE
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