- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00745784
Prolonged Grief in Young Bereaved Spouses and Partners
August 17, 2011 updated by: Memorial Sloan Kettering Cancer Center
Lost to Cancer: Prolonged Grief in Young Bereaved Spouses and Partners
The purpose of the research is to learn more about the experience of grief in young bereaved spouses/partners.
Recent research has shown that young bereaved spouses/partners experience grief uniquely from other age groups, but it is still unclear how certain factors affect the experience of grief.
The investigators research team is interested in studying how the psychological factors of trauma, personality, and meaning of the loss affect grief reactions in young spouses/partners after the loss of a spouse to cancer.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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New York
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Bronx, New York, United States, 10462
- Calavery Hospital
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New York, New York, United States, 10065
- Memorial Sloan Kettering Cancer Center
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 49 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Only spouses/partners of deceased Calvary and Memorial Sloan Kettering patients will be assessed in this study.
Description
Inclusion Criteria:
- Participants must be at least 20 years old and no older than 49 years and 11 months old.
- Participants must have lost a spouse/domestic partner to cancer 6 months to 3 years earlier.
- Participants must be able to give informed consent.
- Participants must be able to comprehend English to complete study assessments.
Exclusion Criteria:
- Major psychopathology or cognitive impairment likely in the judgment of the research staff to interfere with the participation or completion of the protocol.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
1
Young spouses/domestic partners (20-49 years old) of cancer patients who have died from cancer.
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Participants will be administered one battery of questionnaires that should take 50- 55 minutes, which may be broken down into two or more segments if necessary.
They may choose to have these questionnaires administered to them in person at the hospital, in person at their home, or via telephone by a trained master's level research assistant.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
To determine the rate and levels of prolonged grief in young bereaved spouses/partners of cancer patients
Time Frame: conclusion of the study
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conclusion of the study
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
To determine associations among prolonged grief, personality characteristics , previous trauma, & subjective meanings of the loss to the bereaved spouse in young bereaved spouses/partners of cancer
Time Frame: conclusion of the study
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conclusion of the study
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To evaluate whether unique themes emerge among those reporting prolonged grief
Time Frame: conclusion of the study
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conclusion of the study
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To evaluate whether unique themes emerge among those reporting obsessive and histrionic personality traits
Time Frame: conclusion of the study
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conclusion of the study
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Sherry Schacter, PhD, Calvary Hospital, Bronx, NY
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2009
Primary Completion (Actual)
August 1, 2011
Study Completion (Actual)
August 1, 2011
Study Registration Dates
First Submitted
September 2, 2008
First Submitted That Met QC Criteria
September 2, 2008
First Posted (Estimate)
September 3, 2008
Study Record Updates
Last Update Posted (Estimate)
August 18, 2011
Last Update Submitted That Met QC Criteria
August 17, 2011
Last Verified
August 1, 2011
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 08-100
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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