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Adolescent and Young Adult Survivor Transition

Adolescent and Young Adult Survivor Transition (AYAST)

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02948712
Acronym
AYAST
Enrollment
2
Registered
2016-10-28
Start date
2017-02-07
Completion date
2022-06-22
Last updated
2022-06-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adolescent and Young Adult Cancer

Keywords

distress, survivorship, transition period

Brief summary

The purpose of this study is to help adolescents and young adult cancer survivors address their psycho-social needs during the transitional period. The transitional period begins at completion of cancer treatment and continues throughout that first year. Patients often report this period can be difficult and distressing in many areas of life. This study will use a simple tool to measure, on a regular basis, the level of distress a young adult may be feeling. Based on this assessment additional mental health support and intervention can be recommended to help cancer survivors cope and enhance their feelings of well-being.

Detailed description

Study Objective: To establish a successful distress based intervention program for adolescent and young adult survivors in the transition period. Study Design and Methods: The type of design for this study is a feasibility pilot study with repeated measure, within group quantitative design. There is no randomization for this study. The patient will be assessed; at baseline, upon completion of therapy, and at regular three month intervals for the first year, for a total of five assessments. After receiving a referral a member of the AYAST team will contact the patient and set up the initial visit.

Interventions

BEHAVIORALDistress Screening Thermometer

Screening took with an overall distress ranging from 0-10 and additional stress items in the areas of practical problems, family problems, emotional problems, spiritual or religious concerns, and physical problems

BEHAVIORALNCCN Guidelines: Distress management

Based on the NCCN Guidelines Version 1.0.2016 which recommend brief screening, evaluation, and treatment of distress

Sponsors

Case Comprehensive Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* Completed cancer treatment within the past three months of all cancer types and stages * Signed, written consent

Exclusion criteria

* Have not completed cancer treatment within the past three months

Design outcomes

Primary

MeasureTime frameDescription
Decrease in distress score according to National Comprehensive Cancer Network (NCCN) Guidelines V 1.0.2016Up to 15 months after initial visitThe study coordinators are using the NCCN Distress Screening Thermometer (DST) to screen patients. This includes a using the combined score of the NCCN DST and the associated problem list containing 39 items The NCCN Distress Thermometer consists a single-item self- report measure of psychological distress, which consists of an 11-point scale with the endpoints labeled No distress (0) and Extreme distress (10)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026