- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01398891
Development of a Positive Psychology Intervention to Reduce Suicide Risk (HOPE)
This pilot study will recruit patients admitted to the inpatient psychiatric unit at MGH for suicidal ideation or a suicide attempt. Inclusion criteria will be broad to increase enrollment rates and obtain information for patients with a wide range of diagnoses and illness severity. Enrolled subjects will complete randomly-selected positive psychology exercises daily (on weekdays) until discharge and will rate the exercises in multiple domains. Subjects' participation will be complete at the end of their admission or when all exercises have been completed, whichever comes first.
Overall, our goal is to assess the acceptability and utility of eight possible positive psychology interventions related to gratitude, optimism, kindness, mindfulness, recollection, and forgiveness in suicidal inpatients.
This is a single-arm study, completed with patients who have been admitted to the hospital for suicidal ideation or a suicide attempt. It is aimed at developing a positive psychology treatment aimed at suicidal patients. The study consists of serial completion of different positive psychology exercises, once daily, during admission, to get subjects' input on their feasibility and impact. This will allow us to work collaboratively to identify the specific exercises that best fit this population. Subjects' participation ends when they are discharged from the hospital. The investigators plan to enroll 30 subjects at MGH (and total) in this study.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Massachusetts
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Boston, Massachusetts, Estados Unidos, 02114
- Massachusetts General Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Adult (age 18 and older) admitted to inpatient psychiatric unit at Massachusetts General Hospital
- Suicidal ideation at time of admission OR
- Admission occurring in context of suicide attempt
- Ability to read and write in English
Exclusion Criteria:
- Psychotic symptoms
- Cognitive disorder
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Positive Psychology Exercises
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At each session, the interventionalist will prepare the subject to complete a randomly-selected positive psychology exercise, lasting approximately 20 minutes, within the next 24 hours.
He or she will describe the rationale for the exercise and the details of the exercise, and will answer any questions.
A sheet with written instructions (matching the verbal instructions) for the exercise will be provided, with space for recording the exercise and an area to provide ratings on the exercise.
On the following day, the interventionalist will review the prior day's exercise (and record whether it was completed).
The exercises will be completed daily on weekdays for a maximum of 8 days.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Completion of exercises
Periodo de tiempo: Every 24 hours until all exercises administered or discharge occurs
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Exercises assigned each day and assessed for completion the next day (a total of eight exercises)
|
Every 24 hours until all exercises administered or discharge occurs
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Optimism
Periodo de tiempo: Baseline and on the date of discharge (average length of admission= 2 weeks)
|
Life Orientation Test-Revised
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Baseline and on the date of discharge (average length of admission= 2 weeks)
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Feasibility and utility of exercises
Periodo de tiempo: Assessed within 24 hours of exercise completion
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Self-report using Likert scale
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Assessed within 24 hours of exercise completion
|
|
Hopelessness
Periodo de tiempo: Baseline and on the date of discharge (average length of admission=2 weeks)
|
Beck Hopelessness Scale
|
Baseline and on the date of discharge (average length of admission=2 weeks)
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2010P002826
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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