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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02250911
Other study ID # 14-208
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2014
Est. completion date August 2018

Study information

Verified date August 2018
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to gather information on how easy it is to implement the workshop, as well as whether individuals find this workshop helpful. In this study, participants will be assigned at random to one of the two study groups. Based on the information we obtain, we hope to develop an easily accessible support service for caregivers.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date August 2018
Est. primary completion date August 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- As per self report, a current caregiver to a patient with any site or stage of cancer

- Age 18 or over

- A score of > 4 on the Distress Thermometer (DT) and indication that this distress is related in some way to the caregiving role

- In the judgment of the investigators and/or consenting professional, able to comprehend English to complete study assessments

- Able to perform informed consent

- Enrollment is open to caregivers with their own current/past cancer histories

Exclusion Criteria:

- Significant psychiatric or cognitive disturbance sufficient, in the investigator's judgment, to preclude providing informed consent.

- As per self report, unable to access a computer with Internet or unable to use a computer with Internet provided by the study

- Participated in the development and refinement of the CCC Workshop (prospective exemption X14-006)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
webcasts

Behavioral:
Assessments

Other:
Usual care


Locations

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

Sponsors (2)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center American Cancer Society, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary feasibility of this novel approach which will be measured by our ability to recruit our target sample and the proportion of participants who complete the CCC Workshop. Additional indices related to this aim (acceptability) will be gathered via both quantitative (entire sample) and qualitative (with a subset of participants randomized to received the CCC Workshop) methods. 2 years
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