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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00745784
Other study ID # 08-100
Secondary ID
Status Completed
Phase N/A
First received September 2, 2008
Last updated August 17, 2011
Start date January 2009
Est. completion date August 2011

Study information

Verified date August 2011
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date August 2011
Est. primary completion date August 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 49 Years
Eligibility 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 Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Behavioral:
in-person or telephone interview
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.

Locations

Country Name City State
United States Calavery Hospital Bronx New York
United States Memorial Sloan Kettering Cancer Center New York New York

Sponsors (2)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center Calvary Hospital, Bronx, NY

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To determine the rate and levels of prolonged grief in young bereaved spouses/partners of cancer patients conclusion of the study No
Secondary 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 conclusion of the study No
Secondary To evaluate whether unique themes emerge among those reporting prolonged grief conclusion of the study No
Secondary To evaluate whether unique themes emerge among those reporting obsessive and histrionic personality traits conclusion of the study No
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