- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02990572
Amish/Mennonite Research Contact Registry
Research Contact Registry for Members of the Amish and Mennonite Communities
Study Overview
Status
Conditions
Detailed Description
The Amish and Mennonite communities of western Pennsylvania are unique because they are isolated both geographically and socially. These groups originally migrated as a small group from Europe. Since this first settlement there have been additional migration events within North America that have resulted in many distinct communities. These events lead to genetic founder effects, genetic bottleneck effects and virtually zero genetic inflow. The result has been an increased burden of genetic disease on these vulnerable communities. Specific founder genes explain the prevalence of different genetic conditions within each community and family group. This means that families and communities will have a clustering of certain genetic conditions, while the prevalence among the Plain people as a whole remains low. Understanding the specific needs of each family and community group is important in order to deliver comprehensive and specialized care. This requires research studies and needs assessments within these communities. Currently this need is being addressed in eastern Pennsylvania by the Clinic for Special Children in Strasburg. This organization has conducted research to improve access and quality of care for these Plain Communities. There is an apparent need for a similar understanding and relationship with the Plain Communities of western Pennsylvania.
Currently, a barrier exists for identifying and ascertaining appropriate individuals within the Plain Community for new research studies. This is largely due to their social and geographical isolation related to religious and cultural practices. Improving research and understanding within Plain Communities has the potential to improve early diagnosis, interventions, and clinical outcomes. Creating an ongoing registry will moderate these barriers and provide a platform for contacting willing members of the Plain Community for participation in future research projects that may positively impact their medical care, as well as the general care in their communities.
This is not a study but a registry. Potential participants will be educated about the intent of the registry, and written informed consent will be obtained to allow for collection and storage of information in the registry for an indefinite period of time. At the time of consent, potential participants will be informed about what it means to be a part of the registry and the potential for contact and recruitment to future research studies.
One-on-one interviews with a clinician, or with primary and co-investigators, will be conducted. This interview may take place in a clinic setting or the participants home or regional environment. The primary goal of the interview will be to collect a detailed family and medical history of each participant. This will be used to build a detailed pedigree of members of this community. Medical information obtained through released medical records will be included in the registry. Basic demographic and contact information will also be included in the registry.
Subjects information will be stored in the host PhenoTips database and data will be regularly undated and reviewed. Participants may be contacted for future research studies.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Lina Ghaloul Gonzalez, MD, PhD
- Email: lina.gonzalez@chp.edu
Study Contact Backup
- Name: Cate Walsh Vockley, MS, LCGC
- Phone Number: 412-692-7349
- Email: Catherine.WalshVockley@chp.edu
Study Locations
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15224
- Recruiting
- Children's Hospital of Pittsburgh
-
Contact:
- Lina Ghaloul Gonzalez, MD, PhD
- Email: lina.gonzalez@chp.edu
-
Contact:
- Cate Walsh Vockley, MS, LCGC
- Phone Number: 412-692-7349
- Email: Catherine.WalshVockley@chp.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Amish and Mennonite men and women age 18 or older
- Amish and Mennonite children with the permission of a parent
Exclusion Criteria:
- Amish and Mennonite men and woman age 18 or older who do not speak English
- Those who are not Amish or Mennonite
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Amish and Mennonite
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Accumulation and clinical definition of a patient population who are willing to participate in future research studies for which they are eligible.
Time Frame: This registry is intended to be an ongoing resource for recruitment into future research studies and will be maintained up to 14 years.
|
This research registry is intended to allow for identification of patients from the Plain Communities who are willing to participate in medical research.
Eligibility for each future study will likely cary and patients will be selected and contacted with their permission, by dint of having consented to this registry, about the option of participating in a new research study.
|
This registry is intended to be an ongoing resource for recruitment into future research studies and will be maintained up to 14 years.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Lina Ghaloul Gonzalez, MD, PhD, University of Pittsburgh
Study record dates
Study Major Dates
Study Start
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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