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A Virtual, Group-Based, Expressive Writing Intervention for Survivors of Adolescent and Young Adult Cancer

M.D. Anderson Cancer Center logo

M.D. Anderson Cancer Center

Status

Enrolling

Conditions

Cancer

Treatments

Behavioral: Behavioral Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06434402
2024-0440
NCI-2024-04531 (Other Identifier)

Details and patient eligibility

About

To learn more about the experiences of adolescent and young adult cancer survivors and investigate whether a group-based writing intervention can help to improve quality of life of adolescent and young adult cancer survivors.

Full description

Primary Objective:

To evaluate the feasibility of a virtual, group-based expressive writing intervention for survivors of adolescent and young adult cancer.

Secondary Objective:

To preliminarily assess the impact of the study for cancer survivors.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 39 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 15 - 39 years at cancer diagnosis
  • Age 18 - 39 years at study entry
  • Diagnosed between 1 and 5 years ago prior to enrollment
  • Can speak, read, and write in English

Exclusion criteria

  • Nonmelanoma skin cancer
  • Major mental health disorder (e.g., schizophrenia or bipolar disorder [determined from patient records or self-disclosure])
  • No internet access.

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 3 patient groups

Emerging adults (ages18-25 years)
Experimental group
Description:
Participants complete questionnaires over 20 minutes about their mood, health, and demographic information at baseline, and 1, and 3 months. Participants are asked to write about their cancer experiences over 20 minutes (non-stop) for 4 weeks.
Treatment:
Behavioral: Behavioral Intervention
Young adults (ages 26-39 years)
Experimental group
Description:
Participants complete questionnaires over 20 minutes about their mood, health, and demographic information at baseline, and 1, and 3 months. Participants are asked to write about their cancer experiences over 20 minutes (non-stop) for 4 weeks.
Treatment:
Behavioral: Behavioral Intervention
General group (ages 18-39 years)
Experimental group
Description:
Participants complete questionnaires over 20 minutes about their mood, health, and demographic information at baseline, and 1, and 3 months. Participants are asked to write about their cancer experiences over 20 minutes (non-stop) for 4 weeks.
Treatment:
Behavioral: Behavioral Intervention

Trial contacts and locations

1

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Central trial contact

Qian Lu, MD,PHD

Data sourced from clinicaltrials.gov

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