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Evaluation of Hoarding Behaviour and Eating Disorders Among Holocaust Survivors and Their Descendants

NCT ID: NCT03772301

Last Updated: 2018-12-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-01-01

Study Completion Date

2022-01-31

Brief Summary

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"Hoarding "is a common behavior among Holocaust survivors and is related to the traumatic events they have experienced, and we assume that storage behavior and eating disorders are related to future generations of Holocaust survivors.

Detailed Description

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Conditions

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Hoarding Disorder

Study Design

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Observational Model Type

ECOLOGIC_OR_COMMUNITY

Study Time Perspective

PROSPECTIVE

Study Groups

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Group 1

At least 200 Jewish Holocaust survivors of the first generation living in Germany and Israel - an equal number in each country

No interventions assigned to this group

Group 2

The second generation, whose parents lived in Europe during the Second World War, now live in Germany (originating from Western and Eastern Europe) - at least 200 participants.

No interventions assigned to this group

Group 3

Third generation of Jewish Holocaust survivors who participated in the first phase, currently living in Germany and Israel - at least 200 participants including at least 100 subjects in each country. These are adults only. The research program does not include children and adolescents

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Jewish Holocaust survivors living in Germany and Israel who have expressed their written and written consent to participate in monitoring and testing, and who are able to answer the research questionnaires.

• Their direct offspring and their children (second and third generation)
2. The control population - non-Jewish subjects who are not the descendants of Holocaust survivors living in Germany who have expressed their written and oral consent to participate in monitoring and testing and who are able to answer the research questionnaires and whose parents were not imprisoned in the camps second.

Exclusion Criteria

* (Participants who do not agree to participate (did not sign informed consent form
* Respondents who are unable to answer interviewer questions
* Non-Jewish subjects whose parents were in camps (ie prisoner camps, labor camps, etc.) during the second war.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hillel Yaffe Medical Center

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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HYMC-0083-18

Identifier Type: -

Identifier Source: org_study_id