- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT03081533
Circle Dance for Family Caregivers of the Elderly With Alzheimer. (CircleCare)
21 de março de 2019 atualizado por: Julimara Gomes dos Santos, Universidade Federal de Sao Carlos
Brazilian Circle Dance Program for Family Caregivers of the Elderly With Alzheimer's Disease (CircleCare): a Single-blind, Parallel-group Randomized Controlled Trial
The primary objective of this research is to compare the effects of a 12-week CircleCare on physical functioning of family caregivers of the elderly with AD.
Effects on cognition, psychosocial and frailty-related aspects (secondary objective).
The acute effect of one circle dance session on mood states (tertiary objective).
This randomized controlled trial will involve 40 family caregivers over 50 years old allocated into a control group or an intervention group of 12-weeks (twice a week, 60 min per session) of CircleCare.
Primary outcomes will include balance, speed of gait, lower limb muscle strength, functional mobility and risk of falls.
Secondary outcomes will include cognition, burden, stress, depression, quality of life and frailty.
Mood states will be a tertiary outcome.
The effects of CircleCare will be verified with an ANOVA two-way test and a multiple comparison test when necessary.
The analyzes will follow an intention-to-treat approach.
The change in moods will be evaluated by the paired t-test.
The level of significance will be set at p<0.05.
This study may guide professionals and health policymakers in deciding whether to implement this type of intervention.
If positive effects are demonstrated, this program can be offered in public health services to other groups, given its low cost.
Visão geral do estudo
Status
Desconhecido
Condições
Intervenção / Tratamento
Tipo de estudo
Intervencional
Inscrição (Antecipado)
40
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
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SP
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Sao Carlos, SP, Brasil, 13566-544
- Recrutamento
- Julimara Gomes dos Santos
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Contato:
- Julimara G Santos, PhD
- Número de telefone: +5533991132227
- E-mail: julimaraefi@yahoo.com.br
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
50 anos e mais velhos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Sim
Gêneros Elegíveis para o Estudo
Tudo
Descrição
Inclusion Criteria:
- 50 years or older.
- Family caregiver for at least 6 months of an elderly person with Alzheimer's disease.
- Ability to walk without the help of another person.
Exclusion Criteria:
- Cardiopulmonary or orthopaedic contraindication to the practice of physical exercise.
- Severe visual or hearing deficiency that impedes participation in the intervention and assessments.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Cuidados de suporte
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
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Experimental: Circle Dance Program (CircleCare)
Caregivers (n=20) allocated to the experimental group will participate in 12-week CircleCare twice a week (24 sessions), for 60 min each session.
The planning and conduction of the intervention will be the responsibility of the researcher, a Fitness Professional with training in Circle Dance, called focalizer.
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Circle Dances derives from folk dances, but their current repertoire encompasses traditional and contemporary dances from diverse nations and cultures around the world.
Most of the choreographies are danced with the participants placed in a circle, holding hands, repeating a pattern of steps to the rhythm of the music.
Outros nomes:
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Sem intervenção: Control group
Caregivers (n=20) of this group will not receive the intervention, participating only in the assessment protocol.
They will be instructed not to initiate any regular exercise program during the study period.
At the end of the study, the same CircleCare applied to the experimental group will be offered to the interested of the control group.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Brazilian Version of the Short Physical Performance Battery
Prazo: Baseline and 12 weeks after randomization.
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Battery tests that evaluate the static balance; the speed of gait and lower limb muscle strength.
Each test ranges from zero to four points, and the total score is obtained by summing the score of each test, ranging from zero to 12 points.
The result can receive the following graduation: 0 to 3 points: incapacity or very poor performance; 4 to 6 points: low performance; 7 to 9 points: moderate performance; 10 to 12 points: good performance.
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Baseline and 12 weeks after randomization.
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Timed Up and Go Test
Prazo: Baseline and 12 weeks after randomization.
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Test that evaluates the basic functional mobility through the time spent to get up from a chair with arms, walk 3 meters and return to the chair, as well as the number of steps required to perform the activity.
The shorter the time to perform the task, the better the mobility index.
The 12.47 second cutoff point will be used as an indicator of the risk of falls.
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Baseline and 12 weeks after randomization.
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Addenbrooke's Cognitive Examination-Revised (ACE-R)
Prazo: Baseline and 12 weeks after randomization
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Portuguese version of the Instrument that evaluates the global cognitive function through individual tests of orientation and attention (18 points), memory (26 points), verbal fluency (14 points), language (26 points) and spatial visibility skills (16 points).
The overall score ranges from zero to 100 points.
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Baseline and 12 weeks after randomization
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Zarit Burden Interview (ZBI)
Prazo: Baseline and 12 weeks after randomization
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An instrument that evaluates the physical, psychological and social impact of the task of caring for a patient with mental illness.
The scale is composed of 22 questions, whose scores can range from 0 to 88 points.
A score below 21 points is classified as no burden; of 21 and 40 points indicate a moderate burden; between 41 to 60, moderate to severe burden and ≥ 61 points, a severe burden.
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Baseline and 12 weeks after randomization
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Brazilian Perceived Stress Scale (BPSS-10)
Prazo: Baseline and 12 weeks after randomization
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PSS-10 is used to assess the level of stress perceived by older adults in the last month.
The final score ranges from 0 to 40, with higher scores denoting a greater degree of perceived stress.
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Baseline and 12 weeks after randomization
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Geriatric Depression Scale (GDS-15)
Prazo: Baseline and 12 weeks after randomization
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Scale composed of 15 negative/affirmative questions that evaluate the presence of depressive symptoms in the elderly.
Scores higher than 5 points indicate the risk of depression.
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Baseline and 12 weeks after randomization
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Quality of Life Scale in Alzheimer's disease (QoL-AD - caregiver's version)
Prazo: Baseline and 12 weeks after randomization
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Scale structured in three versions that relate to the quality of life of the elderly, careAn instrument adapted, translated and validated for the Brazilian culture to assess the quality of life of caregivers and elderly with AD.
In this version the caregiver to assess his/her own quality of life.
The score ranges from 13 to 52 points and the lower the score worse is the quality of life.
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Baseline and 12 weeks after randomization
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Frailty Phenotype
Prazo: Baseline and 12 weeks after randomization
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A battery of tests proposed by Fried et al. (2001) that asses unintentional weight loss (10 lbs in the past year), self-reported exhaustion, weakness (grip strength), slow walking speed, and low physical activity.
Participants with three or more criteria will be classified as frail.
Those with one or two criteria, pre-frail.
"No frail" will correspond to the absence of these criteria.
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Baseline and 12 weeks after randomization
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Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Illustrated and Reduced Mood States List (MSL-IR)
Prazo: After randomization, at the beginning and end of the first CircleCare session.
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Scale that evaluates the intensity of positive and negative moods represented by 14 "smile" faces.
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After randomization, at the beginning and end of the first CircleCare session.
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
6 de setembro de 2017
Conclusão Primária (Antecipado)
14 de junho de 2019
Conclusão do estudo (Antecipado)
1 de julho de 2019
Datas de inscrição no estudo
Enviado pela primeira vez
2 de março de 2017
Enviado pela primeira vez que atendeu aos critérios de CQ
10 de março de 2017
Primeira postagem (Real)
16 de março de 2017
Atualizações de registro de estudo
Última Atualização Postada (Real)
25 de março de 2019
Última atualização enviada que atendeu aos critérios de controle de qualidade
21 de março de 2019
Última verificação
1 de março de 2019
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Outros números de identificação do estudo
- 62112716.8.0000.5504
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Descrição do plano IPD
At the end of the study, caregivers will be individually informed about their performance in the assessments, but your personal data will not be shared with others, respecting your privacy and anonymity.
However, the analyzed results will be published in papers, reported in congresses and special interest groups such as groups of Alzheimer's caregivers and health units interested in implementing the circle dances as a health promotion activity.
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .