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Group Curriculum for Improving Survivorship Outcomes in Adolescent and Young Adult Cancer Survivors

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Mayo Clinic

Status

Enrolling

Conditions

Malignant Solid Neoplasm
Hematopoietic and Lymphoid System Neoplasm

Treatments

Other: Quality-of-Life Assessment
Other: Questionnaire Administration
Other: Informational Intervention
Other: Counseling
Other: Medical Chart Review
Procedure: Discussion

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05584449
NCI-2022-07825 (Registry Identifier)
21-007844 (Other Identifier)

Details and patient eligibility

About

This clinical trial studies the effectiveness of a group curriculum in improving survivorship outcomes in adolescent and young adult (AYA) cancer survivors. Many AYA survivors typically do not feel prepared to re-enter "daily life" and would likely benefit from structured interventions to offer education and support in a timely manner as to prepare them for the challenges of life in survivorship. A 6-week group curriculum, designed to specifically meet the needs of AYA cancer survivors and facilitated by licensed social workers, may meet the unique needs of young adults who have survived a cancer diagnosis, and if so, the curriculum could be licensed and used across Mayo Clinic sites and potentially at other cancer centers nationwide.

Full description

PRIMARY OBJECTIVES:

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.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 39 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-39
  • 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

  • Inability to read/write/speak English
  • 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

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

Supportive Care (group curriculum)
Experimental group
Description:
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.
Treatment:
Other: Medical Chart Review
Procedure: Discussion
Other: Informational Intervention
Other: Counseling
Other: Questionnaire Administration
Other: Quality-of-Life Assessment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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