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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05350007
Other study ID # CANFRADE
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 25, 2022
Est. completion date December 31, 2022

Study information

Verified date June 2022
Source Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
Contact Elif Yildirim Ayaz, M.D.
Phone +905325148300
Email drelifyildirim@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to evaluate tanatophobia and rumination in individuals over 65 years of age receiving cancer chemotherapy and to determine the related factors.


Description:

No studies were found in the literature evaluating the relationship between frailty and lack of social support with tanatophobia and rumination. The aim of this study is to evaluate tanatophobia and rumination in individuals over 65 years of age receiving cancer chemotherapy and to determine the related factors.


Recruitment information / eligibility

Status Recruiting
Enrollment 180
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - 65 years or older - Conscious and no communication problems - Being literate - Willing to participate in our study voluntarily - Cancer patient receiving active chemotherapy treatment Exclusion Criteria: - Not being willing to participate in the research - Serious life-threatening condition (critical illness, intensive care unit stay, acute complication) - Dementia, Alzheimer's, cognitive dysfunction - Major psychiatric illness

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Sultan Abdülhamid Training and Research Hospital Üsküdar Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rumination Evaluation of rumination in patients over 65 years of age receiving cancer chemotherapy 1 week
Primary Tanatophobia Evaluation of tanatophobia in patients over 65 years of age receiving cancer chemotherapy 1 week
Secondary fraility Evaluation of fraility in patients over 65 years of age receiving cancer chemotherapy 1 month
Secondary lack of social support Evaluation of lack of social support in patients over 65 years of age receiving cancer chemotherapy 1 month
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