Group Curriculum for Improving Survivorship Outcomes in Adolescent and Young Adult Cancer Survivors
NCT ID: NCT05584449
Last Updated: 2025-09-03
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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RECRUITING
NA
60 participants
INTERVENTIONAL
2023-01-16
2027-10-18
Brief Summary
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Detailed Description
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I. Social workers will develop a curriculum to facilitate psychoeducational, skill-based, and process-oriented group for patients who have entered survivorship.
II. To determine if a specific 6 weeklong psychoeducational, skill-based, and process-oriented peer group curriculum results in improved quality of life for adolescents and young adult cancer survivors.
III. To demonstrate the feasibility of this curriculum to address the needs of this population.
OUTLINE:
Participants attend an online group facilitated by two oncology social workers and receive information regarding coping with cancer survivorship as a young adult, as well as discuss survivorship issues/concerns with peers.
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 (group curriculum)
Participants attend an online group facilitated by two oncology social workers and receive information regarding coping with cancer survivorship as a young adult, as well as discuss survivorship issues/concerns with peers.
Counseling
Attend online group facilitated by two oncology social workers
Discussion
Discuss survivorship issues/concerns
Informational Intervention
Receive young adult cancer survivorship information
Medical Chart Review
Ancillary studies
Quality-of-Life Assessment
Ancillary studies
Questionnaire Administration
Ancillary studies
Interventions
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Counseling
Attend online group facilitated by two oncology social workers
Discussion
Discuss survivorship issues/concerns
Informational Intervention
Receive young adult cancer survivorship information
Medical Chart Review
Ancillary studies
Quality-of-Life Assessment
Ancillary studies
Questionnaire Administration
Ancillary studies
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Is a patient of Mayo Clinic Arizona for oncologic care and/or follow-up
* History of cancer diagnosis
* Treated with curative intent
* Completed cancer treatment within 6 months to 2 years prior to group attendance
* Ability to read/write/speak English
* Ability to participate in a group setting
* Ability to commit to attending all six group meetings
Exclusion Criteria
* No internet or computer access
* Not receiving care at Mayo Clinic Arizona
* Currently receiving treatment for cancer
* Is unable to sit comfortably for 90 minutes
* Was not treated with curative intent
* Is on hospice care
* Co-morbid systemic illness or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessments
18 Years
39 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Principal Investigators
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Melody A Griffith, MSW, LISW
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Arizona
Scottsdale, Arizona, United States
Countries
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Facility Contacts
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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NCI-2022-07825
Identifier Type: REGISTRY
Identifier Source: secondary_id
21-007844
Identifier Type: -
Identifier Source: org_study_id
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