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Motivational Interviewing and Subgingival Instrumentation Outcomes in Periodontitis

1 de junho de 2026 atualizado por: Postgraduate Institute of Dental Sciences Rohtak

Effect of Motivational Interviewing on the Outcomes of Subgingival Instrumentation in Patients With Periodontitis

Motivational Interviewing (MI) represents a patient centered counselling approach designed to facilitate behaviour change by guiding patients through the exploration and resolution of ambivalence toward positive health actions. Adapting OARS microskills (open ended questions fostering dialogue, affirmations building self-efficacy, reflective listening mirroring emotions, summarization making commitments) intertwined with the RULE framework (resisting the righting reflex, understanding personal motivations, empathic listening, empowering autonomy) helps cultivate patient's intrinsic motivation for sustained oral hygiene adherence. It effectively resolves ambivalence toward plaque control behaviours essential for periodontitis management. Grounded in MI's core spirit of equal partnership, evocation of inner values, acceptance and compassionate support, this approach fosters long term adherence to treatment. This is in contrast to oral hygiene instructions that typically employ a directive advice giving method, where clinicians provide patients with prescriptive guidance on maintaining optimal oral hygiene practices. Periodontitis staging, as defined by the 2017 World Workshop classification, delineates disease severity (Stages I-III), complexity of management, and extent of involvement, while grading (A-C) offers a prognostic indicator of the risk for future progression based on factors such as rate of advancement and responsiveness to therapy. Integrating motivational interviewing (MI) with periodontitis staging and grading creates a structured framework from diagnosis to patient centered action, enhancing adherence to stage specific treatment plans. This study seeks to investigate the influence of MI on Clinical outcomes, Patient motivation, Patient related outcomes and Patient's Self-efficacy in oral hygiene following subgingival instrumentation among patients stratified by periodontitis stage. By doing so, it aims to explore the potential of behavior change interventions to yield not only clinical improvements but also broader health benefits in the management of periodontitis.

Visão geral do estudo

Descrição detalhada

Periodontitis is a chronic multifactorial inflammatory disease associated with dysbiotic plaque biofilms and characterized by progressive destruction of the tooth-supporting apparatus. Periodontal disease can cause physical discomfort and contribute to functional limitations, which in turn affect psychological well-being and self-esteem. Periodontitis poses a significant public health challenge due to its high prevalence and potential to cause tooth loss, disability, and impairments in chewing function and aesthetics. Sustaining periodontal health demands patient led interventions, including self-care practices and attention to lifestyle factors. Interventions based on health behaviour change models to target improvements in patient self-efficacy, enhances treatment adherence and increases the frequency of brushing and flossing. Behavioural determinants related to impaired periodontal health includes inadequate plaque control measures, smoking habits, sedentary living, excess alcohol, stress and detrimental eating behaviours. Although subject to modification, these lifestyle factors still generate substantial disease prevalence and economic demands globally.Motivational interviewing (MI) for periodontology is recommended by 1st European workshop on periodontal education, to enhance patient's intrinsic motivation. MI has been found to be effective in treating a broad range of health-related lifestyle problems, such as substance abuse, obesity, diabetes management, tobacco cessation, and poor adherence to medication regimens.

MI was first described in 1983, by Psychologist William R Miller. It was initially developed as a short term approach for problem drinking. Motivational Interviewing is a person centered counselling approach for eliciting behaviour change by helping clients to explore and resolve ambivalence. MI works by activating patients' own motivation for change and adherence to treatment.

The effective implementation of Motivational Interviewing (MI) depends on the practitioner's expertise in essential micro skills (OARS) i.e, Open-ended questions which promotes conversation between the clinician and patient encouraging patient to speak and the clinician listens; Affirmations that recognize the challenges in behaviour change while promoting patient self-efficacy by validation of their strengths; Reflective listening accounts for understanding patient's expressed thoughts and emotions and Summarization that illustrates the clinician's active listening to the patient and offers a brief outline of the discussion, while also aiding in addressing ambivalence. These OARS skills are used within "RULE" framework i.e- Resisting the righting reflex by suppressing the urge to correct or direct the patients as arguing for change evokes counter arguments from patients. Understanding patient's own motivation by exploring patients' perceptions about their current situations and their own reasons for change rather than clinician imposing their own. Listening to patient with empathy over informing to grasp the patient's perspective and help resolve ambivalence about change. Empowering the patient to support their autonomy and self-efficacy enabling them to envision and pursue solutions.

Given the importance of Patient's education and awareness about their periodontal health, this study seeks to investigate the impact of MI on the outcomes of subgingival instrumentation in patients with periodontitis. It also evaluates MI's effects on patient-reported outcomes, motivation, and self-efficacy. By addressing these gaps, the study aims to offer evidence based insights for enhancing periodontal therapy.

Tipo de estudo

Intervencional

Inscrição (Estimado)

66

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.

Contato de estudo

Estude backup de contato

  • Nome: Dr. Rajinder Kumar Sharma, MDS
  • Número de telefone: +919416358222
  • E-mail: rksharmamds@yahoo.in

Locais de estudo

    • Haryana
      • Rohtak, Haryana, Índia, 124001
        • Post Graduate Institute of Dental Sciences, Rohtak
        • Contato:

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

  • Adulto

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

• Systemically healthy Patients with age group 30-50 years diagnosed with (Stage I-III) periodontitis.

Exclusion Criteria:

  • Systemic diseases that may affect periodontal disease progression or outcome of treatment
  • Patients on long term antibiotics
  • Pregnant and lactating women
  • Female patients with history of menopause
  • Current orthodontic treatment or planning to undergo orthodontic treatment during study

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: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Motivation Interviewing
Participants will receive a single session of motivational interviewing
A single individual motivational interviewing session will be delivered to each patient at baseline and 1 month
Comparador Ativo: Oral hygiene Instructions
General oral hygiene instructions will be given to all the patients in control group at baseline and at 1 month
Oral hygiene instructions will be provided to each patient at baseline and at 1 month.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
The Dental Treatment Motivation Scale (DTMS)
Prazo: Baseline, 3 month, 6 month
The Dental Treatment Motivation Scale (DTMS)19 questionnaire will be used to measure each participant's level of motivation. . The scale has a total of 15 items, which assess intrinsic (seven questions) and extrinsic motivation (eight questions). Answers provided on a scale are from 1 to 5, where 1 = "strongly disagree" and 5 = "strongly agree." Patients will complete the questionnaire at the 3, 6 month follow-up appointment after periodontal treatment. Higher score indicates higher level of patient motivation towards dental treatment.
Baseline, 3 month, 6 month
Patient related outcome Measure
Prazo: Baseline, 3 month, 6 month
The Oral Health Impact Profile-14 (OHIP-14) questionnaire will be used to measure each participant's Oral Health related quality of life (OHRQoL). It evaluates 14 questions under seven domains: functional limitation, physical pain, psychological discomfort, physical disability, psychological disability, social disability, and handicap. Each item is scored on a 5-point Likert scale (1=never to 5=very often) with total scores ranging from 0-56 (higher scores indicate worse Oral health quality of life).
Baseline, 3 month, 6 month
Evaluation of Patient's Self Efficacy
Prazo: Baseline, 3 month, 6 month
The Oral Hygiene Related Self Efficacy Scale (OHSE) questionnaire will be used for assessing self-efficacy. It includes 19 items rated on 4 point Likert scale from (1) Completely confident not to (4) Completely confident. Higher scores indicate stronger belief in one's ability to maintain oral health, correlating with better hygiene practices and treatment outcomes.
Baseline, 3 month, 6 month

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Diretor de estudo: Dr. Rajinder Kumar Sharma, MDS, Post Graduate Institute of Dental Sciences, Rohtak

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 (Estimado)

26 de junho de 2026

Conclusão Primária (Estimado)

27 de junho de 2027

Conclusão do estudo (Estimado)

27 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

24 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

24 de maio de 2026

Primeira postagem (Real)

1 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

3 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de junho de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

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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