Research Participant Registry "Hopkins Opportunities for Participant Engagement" (HOPE Registry)
"HOPE" Research Participant Registry "Hopkins Opportunities for Participant Engagement"
The HOPE (Hopkins Opportunities for Participant Engagement) Research Registry is a free and secure way for adults to learn about research studies at Johns Hopkins and find out about opportunities to participate. HOPE was created to help connect people who are interested in research with Johns Hopkins research teams conducting studies in many different health areas.
Adults age 18 or older who live in the United States may voluntarily join HOPE. To enroll, participants complete a short form that takes about 5 minutes and provide basic information about themselves and the types of research the participant may be interested in. Participants may receive information about new research studies, including studies related to the topics selected.
If a participant is interested in a study, the participant can choose to share contact information with the research team so the team can contact the participant directly. Joining HOPE does not mean that a person has to participate in any research study. Participation in HOPE is voluntary, there is no cost to join, and participants can update information or leave the registry at any time.
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
The HOPE (Hopkins Opportunities for Participant Engagement) Research Registry is a free, secure, disease-agnostic research recruitment registry designed to connect adults who are interested in research with research opportunities at Johns Hopkins University. The registry was established to provide a centralized resource where individuals can learn about Johns Hopkins research studies and, if interested, choose to be contacted by research teams.
HOPE is a dynamic registry, meaning that individuals may join on an ongoing basis and may update information or remove themselves from the registry at any time. The registry is intended to support recruitment for Johns Hopkins research studies that have appropriate Institutional Review Board (IRB) approval. HOPE is not itself a research study requiring participants to participate in a specific research intervention or procedure.
Participant information is securely stored and managed within the Johns Hopkins REDCap system. Access to identifiable information is limited to authorized personnel who are approved on the relevant IRB protocols and have completed required privacy training. Study teams using HOPE for recruitment receive limited access to information necessary to contact individuals who have expressed interest in the specific study.
The primary risk associated with joining HOPE is a potential loss of confidentiality of the personal information provided to the registry. Measures are in place to reduce this risk, including secure data storage, controlled access, required privacy training, and routine review of data access and security. There are no medical risks associated with participating in the registry.
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Foujan Moghimi, MSPH
- Número de teléfono: 667-306-9348
- Correo electrónico: fmoghim2@jh.edu
Ubicaciones de estudio
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Maryland
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Baltimore, Maryland, Estados Unidos, 21202
- Johns Hopkins ICTR SOM
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Contacto:
- Foujan Moghimi, MSPH
- Número de teléfono: 667-306-9348
- Correo electrónico: fmoghim2@jh.edu
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-
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
The study population consists of adults age 18 or older who reside in the United States and are interested in learning about research opportunities and/or receiving information about research studies at Johns Hopkins. Participants may include Johns Hopkins patients as well as members of the general community.
Descripción
Inclusion Criteria:
- Age 18 years or older
- Resides in the United States
- Apple to provide informed consent
- Interested in learning about research opportunities and/or receiving research updates
- Able to read English
Exclusion Criteria:
- Under 18 years of age
- Unable to provide informed consent
- Resides outside of the United States
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Modelos observacionales: OTHER
- Perspectivas temporales: OTHER
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of individuals enrolled in the HOPE Research Registry
Periodo de tiempo: Ongoing throughout the duration of the registry, 5 years
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The number of individuals who voluntarily enroll in the HOPE Research Registry after completing the required consent process. Enrollment will be monitored as an ongoing measure of the reach and use of the registry. |
Ongoing throughout the duration of the registry, 5 years
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of registry participants who share contact information with a research team
Periodo de tiempo: Ongoing throughout the duration of the registry, 5 years
|
The number of HOPE participants who explicitly indicate interest in an IRB-approved research study and choose to share demographic and contact information with the study research team. This measure will be used to evaluate participant engagement with research opportunities provided through HOPE. |
Ongoing throughout the duration of the registry, 5 years
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Colaboradores
Colaboradores
Investigadores
Investigadores
- Investigador principal: Daniel Ford, MD, Johns Hopkins University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
Otros números de identificación del estudio
- IRB00556658
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Individual participant data (IPD) collected through the HOPE Research Registry will not be routinely shared with external researchers. HOPE participants' demographic, contact, and research-interest information will only be shared with a Johns Hopkins research team when the participant explicitly indicates interest in a specific IRB-approved study and chooses to share their information with that research team. Shared information may include the participant's name, contact information, race, gender, ethnicity, and other relevant registry information provided by the participant.
Marco de tiempo para compartir IPD
Start Date: July 17, 2026 End Date: Ongoing IPD and supporting information will be available on an ongoing basis throughout the duration of the HOPE Research Registry. IPD will be shared with authorized Johns Hopkins research teams only when a participant explicitly indicates interest in an IRB-approved study and chooses to share their information.
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- SAVIA
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.
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. .