Psycho-Educational Program in Increasing Knowledge and Satisfaction and Decreasing Distress in Younger Patients With Cancer Receiving Treatment
NCT ID: NCT01817335
Last Updated: 2015-06-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
22 participants
INTERVENTIONAL
2013-08-31
2015-05-31
Brief Summary
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Detailed Description
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I. Providing a psycho-educational group to young adults while examining the feasibility of such a group with patients on treatment.
II. Examining effectiveness of the program through evaluating pre-post changes in participant distress, evaluating increases in participant' knowledge regarding disease issues and coping, and evaluating participant satisfaction.
OUTLINE:
Patients undergo psycho-educational program comprising medical/symptom management and communication with a medical team, coping skills, self image, and relationships and communication for 1.5 hours once weekly for 6 weeks.
After completion of study treatment, patients are followed up for 30 days.
Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Supportive care (psycho-educational program)
Patients participate in a psycho-educational program focused on medical/symptom management and communication with a medical team, coping skills, self image, and relationships and communication for 1.5 hours once weekly for 6 weeks.
psychosocial assessment and care
Participate in psycho-educational program
educational intervention
Participate in psycho-educational program
communication skills training
Participate in psycho-educational program
questionnaire administration
Ancillary studies
Interventions
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psychosocial assessment and care
Participate in psycho-educational program
educational intervention
Participate in psycho-educational program
communication skills training
Participate in psycho-educational program
questionnaire administration
Ancillary studies
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Inpatient or outpatient
* Cancer diagnosis
* Physician approval
* Informed consent
Exclusion Criteria
* Currently off treatment (longer than 2 weeks at the time of enrollment)
* In isolation or with isolation precautions
* Non-English speaking
18 Years
30 Years
ALL
No
Sponsors
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National Cancer Institute (NCI)
NIH
City of Hope Medical Center
OTHER
Responsible Party
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Principal Investigators
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Jeanelle Folbrecht
Role: PRINCIPAL_INVESTIGATOR
City of Hope Medical Center
Locations
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City of Hope Medical Center
Duarte, California, United States
Countries
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Other Identifiers
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NCI-2013-00589
Identifier Type: REGISTRY
Identifier Source: secondary_id
13128
Identifier Type: -
Identifier Source: org_study_id
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