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Educação em Saúde Oral para Idosos: Intencionalidade em Ação

20 de setembro de 2026 atualizado por: Mackay Memorial Hospital

Explorar a Eficácia da Intencionalidade da Matriz de Cura na Melhoria dos Resultados da Educação para a Saúde Oral para Pessoas de Meia-Idade e Idosos Residentes na Comunidade

After obtaining approval from the Institutional Review Board (IRB), the clinical trial will be registered on a designated trial registration website. Participant recruitment will be conducted online. For individuals who meet the inclusion criteria and express interest, the principal investigator will verbally explain the study protocol, go over the informed consent form, and answer any related questions. Potential participants who meet the inclusion criteria and are willing to participate will be given time to consider their involvement in the study.

Inclusion criteria for this study are:

  1. Adults aged 40 and older
  2. Ability to hear, speak, and read Chinese, and communicate fluently in Mandarin or Taiwanese.

Exclusion criteria include:

  1. Being completely edentulous and not using dentures;
  2. Having severe food allergies, renal failure, or dysphagia;
  3. Being diagnosed with terminal illness under palliative care, severe mental illness, or cognitive impairment;
  4. Having a serious health condition that prevents standing or performing oral self-care behaviors.

Upon receiving verbal agreement from potential participants, the study procedure and the contents of the consent form will be explained again. This is a parallel randomized experimental study, with an estimated sample of 90 middle-aged and older adults recruited from the community through online means. Participants will be randomly assigned to one of three groups:

  1. intentional interviews combined with expressive arts activities,
  2. expressive arts activities only, or
  3. control group.

All three groups will receive oral health education before the intervention and six weeks after the intervention. Questionnaire surveys will be conducted one week and one month post-education to collect data on sarcopenia risk, eating assessment, grit, oral health literacy, and oral self-care behaviors. Statistical analyses will be performed on the collected data.

Participants who fully understand the study and agree to participate will sign an informed consent form. Two copies of the consent form will be prepared-one will be kept by the principal investigator, and a photocopy will be given to the participant for personal recordkeeping. Participants retain the right to decline or withdraw from the study at any time, even after signing the consent form. Their withdrawal will not affect their future rights, benefits, or services, and any previously collected data will be deleted upon request.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Real)

76

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

    • New Taipei City
      • New Taipei City, New Taipei City, Taiwan
        • Sanzhi

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

40 anos a 100 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  1. Individuals aged 40 years or older (Vlietstra et al., 2024).
  2. Ability to hear, speak, and read Chinese, with no communication barriers in Mandarin or Taiwanese.

Exclusion Criteria:

  1. Edentulous individuals who do not use dentures.
  2. Individuals with severe food allergies, renal failure, or dysphagia.
  3. Individuals diagnosed with terminal illness under palliative care, severe psychiatric disorders, or cognitive impairments.
  4. Individuals with serious medical conditions that prevent standing or performing oral self-care behaviors.

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: Pesquisa de serviços de saúde
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Sem intervenção: Control Group

Participants in the control group will not receive any intentional interview or expressive arts activity during the 6-week intervention period. They will receive oral health education after the same time interval as the experimental arms, ensuring consistency in outcome measurement.

Comparador Ativo: Expressive Arts Activities Only

Participants in this arm will engage only in expressive arts activities over a 6-week period. These activities are designed to foster creative engagement and emotional well-being. After the intervention, participants will receive the same oral health education provided to all groups.

Participants in this arm will receive an intervention

Experimental: Intentional Interview + Expressive Arts Activities

Participants in this arm will receive an intervention combining an intentional interview based on the Intentionality Matrix of Healing framework with expressive arts activities. The intentional interview is designed to guide participants in reflecting on personal health-related intentions, while the expressive arts component facilitates emotional expression and engagement. After the 6-week intervention, all participants will also receive standardized oral health education.

Participants in this arm will receive an intervention

Participants in this arm will engage only in expressive arts activities over a 6-week period.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
sarcopenia risk
Prazo: baseline, one week after the intervention, and at a one-month follow-up

This study adopted the SARC-F questionnaire proposed by the Asian Working Group for Sarcopenia (AWGS). The tool consists of five questions aimed at assessing muscle function, including grip strength, endurance, walking ability, ability to stand up from a chair, and fall history in the past six months (Ishida et al., 2020). The first four items are scored based on the responses: no difficulty (0 points), some difficulty (1 point), and a lot of difficulty (2 points). The fifth item, fall history, is scored as follows: 0 falls = 0 points, 1-3 falls = 1 point, and 4 or more falls = 2 points. The total score ranges from 0 to 10, with higher scores indicating a greater risk of sarcopenia. A SARC-F score of 4 or higher suggests a positive result for self-screening, indicating the need for further medical evaluation and appropriate diagnostic and treatment interventions.

The sensitivity, specificity, and positive/negative likelihood ratios of the SARC-F for predicting sarcopenia and its risk

baseline, one week after the intervention, and at a one-month follow-up
eating assessment
Prazo: baseline, one week after the intervention, and at a one-month follow-up

This study utilized the Eating Assessment Tool-10 (EAT-10), a dysphagia screening tool included in the adult oral health assessment form issued by the Department of Oral Health, Ministry of Health and Welfare. The version used is the Chinese translation by Huang (2023) of the original tool developed by Belafsky et al. (2008). The EAT-10 consists of 10 items that assess self-perceived difficulties related to swallowing, encompassing physical, psychological, and social aspects. Example items include: "Swallowing problems have caused me to lose weight" and "Swallowing interferes with my ability to go out for meals." The scale has demonstrated good reliability and validity, with a Cronbach's alpha coefficient of 0.92. The total score ranges from 0 to 40, with a score of ≥3 indicating the presence of swallowing difficulties. Higher scores reflect a greater risk of oral frailty.

baseline, one week after the intervention, and at a one-month follow-up
grit
Prazo: baseline, one week after the intervention, and at a one-month follow-up

This study adopted the Chinese version of the Grit Scale (Grit-10) developed by Duckworth et al. (2009). The scale consists of 10 items across two main factors: passion (reverse-scored items) and perseverance. Example items include: "I often set a goal but later choose to pursue a different one" (passion, reverse-scored) and "I finish whatever I begin" (perseverance). The scale uses a 5-point Likert rating system, ranging from 1 (not at all like me) to 5 (very much like me).

Scoring is as follows: each item has a maximum score of 5. Odd-numbered items are reverse scored, and even-numbered items are positively scored. The total score of the odd-numbered items divided by 5 gives the passion subscale score, while the total score of the even-numbered items divided by 5 gives the perseverance subscale score. The sum of all 10 items divided by 10 yields the overall grit score.

Lin (2019) applied this Chinese version to university students and reported a Cronbach's alpha of 0.84 for the ov

baseline, one week after the intervention, and at a one-month follow-up
oral health literacy
Prazo: baseline, one week after the intervention, and at a one-month follow-up

This study adopted the short-form Health Literacy Dental Scale (HeLD-14) developed by Jones et al. (2015), which has a Cronbach's alpha of 0.87. The scale was translated into Simplified Chinese by Liu et al. (2021) (Chinese version of HeLD, HeLD-C), showing a Cronbach's alpha of 0.92, and was later adapted into a Traditional Chinese version by Cheng (2023). The Traditional Chinese version includes 13 items across seven domains:

Receptivity (e.g., "I care about my dental or oral health needs"),

Understanding (e.g., "I can fill out dental-related forms"),

Support (e.g., "I can bring family members or friends to dental visits"),

Economic Barriers (e.g., "I can afford the cost of dental or oral health care"),

Utilization (e.g., "I know how to make a dental appointment"),

Communication (e.g., "I can obtain alternative oral health opinions from other dentists"), and

Access to Resources (e.g., "I can follow the dentist's instructions").

The scale uses a 5-point Likert rating system r

baseline, one week after the intervention, and at a one-month follow-up
oral self-care behaviors
Prazo: baseline, one week after the intervention, and at a one-month follow-up

This study adopted the Oral Self-Care Behavior Scale revised by Cheng (2023), originally developed by Ho, Rita Chang et al. (2019). The scale consists of 10 items; example statements include: "I brush my teeth at least twice a day" and "I always brush my teeth before going to bed at night." A 4-point Likert scale is used, ranging from 1 (not at all) to 4 (completely). The total score ranges from 10 to 40, with higher scores indicating better oral self-care behavior. The Cronbach's alpha ranges from 0.78 to 0.87 (Cheng, 2023), demonstrating good reliability.

baseline, one week after the intervention, and at a one-month follow-up

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)

2 de julho de 2025

Conclusão Primária (Real)

17 de dezembro de 2025

Conclusão do estudo (Real)

29 de maio de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

13 de junho de 2025

Enviado pela primeira vez que atendeu aos critérios de CQ

24 de novembro de 2025

Primeira postagem (Real)

5 de dezembro de 2025

Atualizações de registro de estudo

Última Atualização Postada (Real)

22 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

20 de setembro de 2026

Última verificação

1 de dezembro de 2025

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 25MMHIS120e

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

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 .

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