An observational study in Hoarding Disorder, sponsored by Hillel Yaffe Medical Center. Status unknown. Per ClinicalTrials.gov, last updated 2018-12-11.
Sponsored by Hillel Yaffe Medical Center · Observational
"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.
32 studies on the registry are indexed under Hoarding Disorder; 5 are open to participants now.
Browse Hoarding Disorder studies →Hillel Yaffe Medical Center is the lead sponsor of 305 studies on the registry; 10 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Jewish Holocaust survivors living in Germany and Israel Their direct offspring and their children (second and third generation)
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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.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
At least 200 Jewish Holocaust survivors of the first generation living in Germany and Israel - an equal number in each country
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.
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
Hoarding
Questionnaire that will follow behaviour over generations
Time frame: Three years
No study locations are listed for this record.
This study is status unknown, as verified in Dec 2018. You cannot join it, but the record below documents what was studied.
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