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Tech-TYA: eHealth Platform to Deliver Group Intervention for YA Cancer Survivors

University of Arizona logo

University of Arizona

Status

Completed

Conditions

Cancer

Treatments

Behavioral: Cognitive-Behavioral Stress Management and Health Education

Study type

Interventional

Funder types

Other

Identifiers

NCT05597228
STUDY00000717

Details and patient eligibility

About

The purpose of this study is to adapt a web-based platform to deliver a group intervention for young adult cancer survivors.

Full description

In the first part of this study, the investigators adapted a website to deliver an evidence-based intervention for improving HRQOL for young adult cancer survivors, and then conducted usability testing sessions with young adult cancer survivors to get feedback on the website. In the second part of the study, the investigators will conduct a single-arm pilot trial in which the website will be used to deliver the intervention via weekly group meetings with a trained facilitator over the course of 10 weeks.

Enrollment

7 patients

Sex

All

Ages

18 to 39 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Aged 18-39 years at the time of participation
  2. Diagnosed with a primary cancer between 18-39 years old
  3. Finished cancer treatment with curative intent 1 month to 5 years prior to enrollment (except hormone therapy)
  4. NED and no anticipated/scheduled anti-cancer treatments at the time of enrollment (except hormone therapy)
  5. Able to speak and read English
  6. Able and willing to give informed consent
  7. Access to internet or cellular connectivity with sufficient bandwidth to participate in videoconferences (Part 2 only)

Exclusion criteria

  1. Ongoing or future anti-cancer treatments (beyond hormone therapy) are scheduled or anticipated
  2. Documented or observable psychiatric or neurological disorders that could interfere with study participation (e.g., psychosis, active substance abuse)

Vulnerable populations will not be included in this study.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

7 participants in 1 patient group

Behavioral: Cognitive-Behavioral Stress Management and Health Education
Experimental group
Description:
Weekly video conference groups led by a trained facilitator
Treatment:
Behavioral: Cognitive-Behavioral Stress Management and Health Education

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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