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.
研究概览
详细说明
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.
研究类型
注册 (估计的)
联系人和位置
学习联系方式
- 姓名:Foujan Moghimi, MSPH
- 电话号码:667-306-9348
- 邮箱:fmoghim2@jh.edu
学习地点
-
-
Maryland
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Baltimore、Maryland、美国、21202
- Johns Hopkins ICTR SOM
-
接触:
- Foujan Moghimi, MSPH
- 电话号码:667-306-9348
- 邮箱:fmoghim2@jh.edu
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
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.
描述
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
学习计划
研究是如何设计的?
设计细节
- 观测模型:OTHER
- 时间观点:OTHER
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of individuals enrolled in the HOPE Research Registry
大体时间:Ongoing throughout the duration of the registry, 5 years
|
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
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of registry participants who share contact information with a research team
大体时间: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
|
合作者和调查者
调查人员
- 首席研究员:Daniel Ford, MD、Johns Hopkins University
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他研究编号
- IRB00556658
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
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.
IPD 共享时间框架
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.
IPD 共享支持信息类型
- 研究方案
- 树液
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.