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Effects of Telephone Intervention and Nudging Information on Cancer Screening Behavior

3 de noviembre de 2026 actualizado por: Chiayi Christian Hospital

Effects of Telephone Intervention and Nudging Information on Cancer Screening Behavior: A Randomized Clinical Study

Objectives: Telephone interventions are often delivered to promote cancer screening for early detection and treatment. However, the effects of nudging information provided in telephone interventions on cancer screening behavior remain unclear. Accordingly, this study investigated the effects of telephone-delivered nudging information regarding screening benefits and social norms on cancer screening behavior.

Methods: This randomized controlled trial included 1,200 community-dwelling individuals meeting screening criteria for colorectal, breast, cervical, or oral cancer. Participants were assigned to one of four groups: telephone benefits, telephone social norms, telephone reminder, and letter reminder. The dependent variable was cancer screening behavior within 6 months after the intervention.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Actual)

1200

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Tainan, Taiwán, 701
        • National Cheng Kung University

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

30 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Community-dwelling individuals who met the criteria for cancer screening outlined by the Health Promotion Administration under Taiwan's Ministry of Health and Welfare were recruited. Participants were required to have sufficient communication ability and the ability to receive a telephone interview.
  • colorectal cancer: people aged 50 to 74 years who have not received a fecal occult blood test within the past 2 years;
  • breast cancer: women aged 45 to 69 years or those aged 40 to 44 years with a family history of breast cancer who have not received a mammography within the previous 2 years;
  • cervical cancer: women aged over 30 years who have not received a pap smear test within the past 3 years; and
  • oral cancer: the general people aged over 30 years or indigenous residents of Taiwan aged over 18 years with a history of chewing betel nut or smoking who have not received an oral mucosal examination within the past 2 years.

Exclusion Criteria:

  • This study did not consider individuals with severe cognitive impairment or a previous cancer diagnosis, as indicated by chart records.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Poner en pantalla
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: telephone benefits group

In the intervention, participants were provided with three categories of information: (1) the reasons why they were receiving the information (delivered by telephone or letter), that is, information regarding the criteria they met, such as their age or lack of screening history within a certain time period; (2) reasons why they should undergo screening, including nudging information related to benefits or social norms; and (3) a description of how they could make cancer screening appointments.

In the telephone benefits group, key information regarding the benefits of cancer screening was provided with consideration of the health belief model (Lau et al., 2020).

Experimental: telephone social norms group

In the intervention, participants were provided with three categories of information: (1) the reasons why they were receiving the information (delivered by telephone or letter), that is, information regarding the criteria they met, such as their age or lack of screening history within a certain time period; (2) reasons why they should undergo screening, including nudging information related to benefits or social norms; and (3) a description of how they could make cancer screening appointments.

In the telephone social norms group, the following were provided with consideration of the theory of planned behavior (Ritchie et al., 2021).

Comparador activo: telephone reminder group

In the intervention, participants were provided with three categories of information: (1) the reasons why they were receiving the information (delivered by telephone or letter), that is, information regarding the criteria they met, such as their age or lack of screening history within a certain time period; (2) reasons why they should undergo screening, including nudging information related to benefits or social norms; and (3) a description of how they could make cancer screening appointments. The telephone reminder group only received the first and third types of information.

Comparador activo: letter reminder group

In the intervention, participants were provided with three categories of information: (1) the reasons why they were receiving the information (delivered by telephone or letter), that is, information regarding the criteria they met, such as their age or lack of screening history within a certain time period; (2) reasons why they should undergo screening, including nudging information related to benefits or social norms; and (3) a description of how they could make cancer screening appointments. The letter reminder group only received the first and third types of information.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Cancer behavior
Periodo de tiempo: From enrollment to the end of treatment at 6 months.

The primary outcome is whether the participants completed cancer screening or not (yes or no)

From enrollment to the end of treatment at 6 months.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

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Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de enero de 2023

Finalización primaria (Actual)

1 de enero de 2023

Finalización del estudio (Actual)

31 de octubre de 2023

Fechas de registro del estudio

Enviado por primera vez

16 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

3 de noviembre de 2026

Publicado por primera vez (Actual)

9 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

9 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

3 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • IRB2021031

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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