IA Trial Radar | ||
|---|---|---|
El ensayo clínico NCT07127731 (REACH BP) para Hypertension (HTN), Hypertension ,Pregnancy, Actividad física está aún no recluta. Consulte la vista de tarjeta del Radar de Ensayos Clínicos y las herramientas de descubrimiento de IA para conocer todos los detalles. O haga cualquier pregunta aquí. | ||
Un estudio coincide con los criterios de filtro
Vista de tarjeta
Volver a la búsqueda
Universidad del NoroesteREmote Physical ACtivity Intervention for High Blood Pressure Postpartum (REACH BP) 60 Posparto Remoto
Los detalles del ensayo clínico están disponibles principalmente en inglés. ¡Sin embargo, IA Trial Radar puede ayudar! Simplemente haga clic en 'Explicar el estudio' para ver y discutir la información del estudio en el idioma que haya seleccionado.
El ensayo clínico NCT07127731 (REACH BP) es un estudio intervencionista para Hypertension (HTN), Hypertension ,Pregnancy, Actividad física. Su estado actual es: aún no recluta. Se prevé iniciar el reclutamiento el 1 de abril de 2027 hasta completar 60 participantes. Dirigido por la Universidad del Noroeste, se espera que finalice el 1 de abril de 2028. Los datos se actualizaron por última vez en ClinicalTrials.gov el 23 de marzo de 2026.
Resumen
The purpose of this intervention is to help new mothers who had elevated blood pressure during pregnancy become more physically active after birth. The investigators will connect data from FitBits to the electronic health record. Women will then get weekly messages with feedback and goals to help them stay active. The investigators will test if the intervention improves step counts and blood pressure after pregnancy....Mostrar más
Título oficial
REACH BP: REmote Physical ACtivity Intervention for High Blood Pressure Postpartum
Condiciones médicas
Hypertension (HTN)Hypertension ,PregnancyActividad físicaOtros ID del estudio
- REACH BP
- STU00224381
- 25CDA1449707 (Otra financiación) (American Heart Association)
Número del NCT
Inicio del estudio (real)
2027-04
Última actualización
2026-03-23
Fecha de finalización (estimada)
2028-04
Inscripción (prevista)
60
Tipo de estudio
Intervencionista
FASE
N/A
Estado general
Aún no recluta
Palabras clave
hypertension
pregnancy
postpartum
physical activity
pregnancy
postpartum
physical activity
Objetivo principal
Tratamiento
Método de asignación
Aleatorizado
Modelo de intervención
Paralelo
Enmascaramiento
Doble ciego
Brazos / Intervenciones
| Grupo de participantes | Intervención/Tratamiento |
|---|---|
ExperimentalExperimental Group | Patient Portal Messaging Participants will receive weekly messages via their patient portal including feedback on their step counts and step count goals based on data from their FitBits FitBit EHR Linkage Participants will receive FitBits and link this step count data with the Electronic Health Record (EHR) |
Comparador activoControl Group | FitBit EHR Linkage Participants will receive FitBits and link this step count data with the Electronic Health Record (EHR) |
Resultado primario
| Medida de resultado | Descripción de la medida | Periodo de tiempo |
|---|---|---|
Feasibility of Recruitment | Number of participants enrolled in the intervention | From enrollment to the end of the 24 week intervention |
Feasibility of Participant Retention | Percent of enrolled participants who continue to participate in the intervention | At study weeks 12 and 24 |
Feasibility of FitBit+EHR linkage | Percent of intervention days FitBit data are linked to the Electronic Health Record | From enrollment to the end of the 24 week intervention |
Feasibility of Intervention Messaging | Percent of weekly messages that are read by participants | From enrollment to the end of the 24 week intervention |
Acceptability of the Intervention | Participants will fill out a survey to assess the extent to which they were satisfied with individual intervention components including FitBit usage, portal messaging, blood pressure and weight assessments, surveys, intervention length and intervention delivery. Each component will be rated on a 5-point Likert Scale in which 1 represents very dissatisfied (lowest score) and 5 represents very satisfied (highest score). | Study week 24 |
Asistente de participación
Criterios de elegibilidad
Criterios de edad
Adulto, Adulto mayor
Edad mínima
18 Years
Criterios de sexo
Mujer
- Delivery of a live birth at Northwestern Medicine 6-12 weeks prior
- Systolic blood pressure 120-139 or diastolic blood pressure 80-89 during the first 20 weeks of gestation
- Low self-reported physical activity levels
- Able to access the internet at least weekly
- Have patient portal account or willing to set one up
- Willing to wear a FitBit
- Spoken and written English or Spanish language fluency
- Medical contraindications to participating in a structured physical activity program
- Currently participating in a structured physical activity or weight loss program
- Hypertensive disorder of pregnancy (e.g., preeclampsia, gestational hypertension, eclampsia)
Universidad del NoroesteInstituto Nacional de Alergias y Enfermedades Infecciosas, Estados Unidos747 estudios activos para explorarParte responsable del estudio
Natalie Cameron, Investigador principal, Instructor, Northwestern University
Contactos centrales del estudio
Contacto: Natalie A Cameron, MD, MPH, 312-503-2137, [email protected]
Sitio no especificado.