- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04279093
Digital Assessment of Well-being in New Parents (DAWN-P)
Digital Assessment of Well-being in New Parents (DAWN-P)
The mental health of new parents around the time of the birth of their baby has been identified as a key priority in the NHS (National Health Service) Long Term plan. At present, there is no nationally implemented method for monitoring parents' mental health, although the use of the Edinburgh Postnatal Depression Scale (EPDS) has been recommended. This is a paper based questionnaire administered by health visitors in the postnatal period. For the purposes of this project, the investigators contacted health visitors in Manchester to find out how they use EPDS in practice. Currently, health visitors only use the questionnaire if they feel there is a need during visits, and the questionnaire is not kept (only the overall score). Since almost 20% of mums develop postnatal depression, more systematic and thorough screening is needed.
The investigators developed an app version of the EPDS which takes less than 2 minutes to complete on a smartphone. It is anticpated that this will be a more accessible and practical method of conducting this important assessment. This project is a feasibility study to find out whether an app would be a feasible, acceptable, valid and safe way to monitor perinatal mental health in women and their partners.
The investigators aim to recruit 20 women and their partners in late pregnancy (after 36 weeks gestation) and ask them to use the app. The app will prompt completion of the EPDS once per day until 6 weeks postnatally. Participants' responses on the app will be transferred to a secure server at the University of Manchester. Participants will be invited to complete a paper version of the EPDS at the beginning and end of the study to check validity. They will also be asked to complete a questionnaire measuring the acceptability of the app and to take part in a brief qualitative interview at the end of the study.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
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Greater Manchester
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Manchester, Greater Manchester, Reino Unido, M13 9PL
- University of Manchester
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
The investigators aim to recruit 20 women in late pregnancy from the Antenatal Assessment Unit and the Antenatal Clinic at St Mary's Hospital, Manchester. Their partners will be invited to participate where applicable.
Inclusion criteria for pregnant women:
- after 36 weeks gestation
- aged over 18 years
- fluent in English
- under the care of Manchester University NHS Foundation Trust
Exclusion criteria for pregnant women:
- current stillbirth (women experiencing a stillbirth during the study will be withdrawn from the study)
- fetal abnormality
- multiple pregnancy
Inclusion criteria for partners:
- male or female partners of a mum participating in the study
- aged over 18
- fluent in English.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Modelos observacionales: Grupo
- Perspectivas temporales: Futuro
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
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Pregnant/postpartum women and their partners
The investigators aim to recruit 20 women in late pregnancy from the Antenatal Assessment Unit and the Antenatal Clinic at St Mary's Hospital. Their partners will be invited to participate where applicable. Inclusion and exclusion criteria for pregnant women are as follows:
Inclusion criteria for partners: male or female partners of a mum participating in the study, aged over 18 and fluent in English. |
No intervention, but participants will use a smartphone app daily (ClinTouch DAWN-P) to complete the Edinburgh Postnatal Depression Scale
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Percentage of app based EPDS (Edinburgh Postnatal Depression Scale) assessments completed during the app-use phase
Periodo de tiempo: 36 weeks gestation until 6 weeks postpartum
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Percentage of app based EPDS (Edinburgh Postnatal Depression Scale) assessments completed during the app-use phase
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36 weeks gestation until 6 weeks postpartum
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Percentage of eligible individuals recruited to the study
Periodo de tiempo: Baseline
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Percentage of eligible individuals recruited to the study
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Baseline
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Dropout rate - percentage of participants who consent to take part in the study dropping out during the app use phase
Periodo de tiempo: 36 weeks gestation until 6 weeks postpartum
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Percentage of participants who consent to take part in the study dropping out during the app use phase
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36 weeks gestation until 6 weeks postpartum
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Percentage of participants completing at least a third of app-based assessments
Periodo de tiempo: 36 weeks gestation until 6 weeks postpartum
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Percentage of participants completing at least a third of app-based assessments.
The a priori "accept" criterion will be >33% data points completed
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36 weeks gestation until 6 weeks postpartum
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Percentage of participants completing at least half of app-based assessments
Periodo de tiempo: 36 weeks gestation until 6 weeks postpartum
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Percentage of participants completing at least half of app-based assessments.
The a priori target criterion will be 50% of participants submitting at least 50% of app-based assessments.
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36 weeks gestation until 6 weeks postpartum
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Transcripts from qualitative interviews with parents who have used the screening app regarding acceptability of the app
Periodo de tiempo: 6 weeks postpartum
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Transcripts from qualitative interviews with parents who have used the screening app regarding acceptability of the app
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6 weeks postpartum
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abridged Mobile App Rating Scale
Periodo de tiempo: 6 weeks postpartum
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abridged Mobile App Rating Scale score
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6 weeks postpartum
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Edinburgh Postnatal Depression Scale - app-based version
Periodo de tiempo: 36 weeks gestation until 6 weeks postpartum
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Edinburgh Postnatal Depression Scale - app-based version
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36 weeks gestation until 6 weeks postpartum
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Edinburgh Postnatal Depression Scale - paper version
Periodo de tiempo: 36-37 weeks gestation; 5-6 weeks postpartum
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Edinburgh Postnatal Depression Scale - paper version
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36-37 weeks gestation; 5-6 weeks postpartum
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Number of adverse events occurring during the app-use phase of the study
Periodo de tiempo: 36 weeks gestation until 6 weeks postpartum
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Number of adverse events occurring during the app-use phase of the study
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36 weeks gestation until 6 weeks postpartum
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Qualitative interview data on participants' experience of using the app.
Periodo de tiempo: 6 weeks postpartum
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Qualitative interview data on participants' experience of using the app.
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6 weeks postpartum
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Demographic questionnaire
Periodo de tiempo: Baseline (36 weeks pregnant)
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Demographic questionnaire asking standard questions about participants' demographic characteristics - e.g.
age, gender, employment status.
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Baseline (36 weeks pregnant)
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BMI (from casenotes)
Periodo de tiempo: Baseline (36 weeks pregnant)
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BMI (from casenotes)
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Baseline (36 weeks pregnant)
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past psychiatric history as reported in casenotes (any history of major depression, previously prescribed psychiatric medication, previously referred for talking therapy)
Periodo de tiempo: Baseline (36 weeks pregnant)
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past psychiatric history as reported in casenotes (any history of major depression, previously prescribed psychiatric medication, previously referred for talking therapy)
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Baseline (36 weeks pregnant)
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Answers to mental health screening questions at booking appointment (NICE, 2014: section 1.5.4)
Periodo de tiempo: Baseline (36 weeks pregnant)
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Answers to mental health screening questions at booking appointment (NICE, 2014: section 1.5.4)
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Baseline (36 weeks pregnant)
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Details of current childbirth (mode of delivery, live/still birth, any major obstetric complications)
Periodo de tiempo: Baseline (36 weeks pregnant)
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Details of current childbirth (mode of delivery, live/still birth, any major obstetric complications)
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Baseline (36 weeks pregnant)
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parity (total number of pregnancies reaching viable gestational age)
Periodo de tiempo: Baseline (36 weeks pregnant)
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parity (total number of pregnancies reaching viable gestational age)
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Baseline (36 weeks pregnant)
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
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 (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 274007
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
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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