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CancerNCT06275854

YASU Research Registry: For Young Adults With Cancer

An observational study of Cancer and Leukemia, run by Young Adult Survivors United at 1 site in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

The goal of this observational research registry is to learn about health, wellbeing, and needs of survivors of young adult cancer (diagnosed between the ages of 18 and 39). The main question[s] it aims to understand are: What are the levels of depression, anxiety, social support, and financial distress Determine… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Cancer, Leukemia, Sarcoma
How many people
192 participants
Where
1 siteUnited States
Study dates
3 Feb 2025to 30 Sep 2025
How long will I take part?
10 Years
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Any young adult diagnosed with cancer between the ages of 18 and 39 willing to register on the YASU website and consents to participation in the research registry.

Who may be able to join

  • Cancer diagnosis received between the ages of 18 and 39.
  • Able to speak and read English

Who cannot join

  • Inability to provide consent (such as neurological illness or mental incapacity)
  • Has not registered as a member of YASU

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Young Adult Survivors United

    Wexford, Pennsylvania, 15090

Other trials in United States

About this study

Official title: Young Adult Survivors United Cancer Research Registry

The goal of this observational research registry is to learn about health, wellbeing, and needs of survivors of young adult cancer (diagnosed between the ages of 18 and 39). The main question[s] it aims to understand are:

  • What are the levels of depression, anxiety, social support, and financial distress
  • Determine effectiveness of YASU programming by measuring changes over time

With this registry, the investigators also plan to identify survivors who may be eligible for participation in future research studies pertaining to young adult cancer.

Participants will be asked to complete electronic surveys every 6 to 12 months during participation in the registry.

Read the detailed description

The study will be conducted online.

Keywords
young adult cancer
Medical subject headings
Neoplasms, Leukemia, Sarcoma, Neoplasms, Germ Cell and Embryonal, Lymphoma, Colorectal Neoplasms, Melanoma, Breast Neoplasms

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Anxiety

    General Anxiety Disorder-7 (GAD-7). Scores range from 0-21 with higher scores indicating higher levels of anxiety.

    Measured: enrollment in registry, 6 months later, yearly until death

  2. Depressive symptoms

    Patient Health Questionnaire- 9 (PHQ-9) Scores range from 0-27, with higher scores indicating more depressive symptoms.

    Measured: enrollment in registry, 6 months later, yearly until death

  3. Social Support

    MOS Social Support Survey Instrument The survey consists of four separate social support subscales and an overall functional social support index. A higher score for an individual scale or for the overall support index indicates more support.

    MOS Social Support Survey Instrument

    Measure of Social Support Survey Instrument

    Measured: enrollment in registry, 6 months later, yearly until death

  4. Financial Toxicity

    COST: A FACIT Measure of Financial Toxicity (COST - FACIT (Ver 2)) Scores range from 0-44. The higher the score, the better the Financial Well-Being

    Measured: enrollment in registry, 6 months later, yearly until death

  5. Needs Assessment

    AYA Psycho-Oncology Screening Tool (AYA-POST) There is no scoring required for this tool.

    Measured: enrollment in registry

Secondary outcomes (1)
  1. Name, address, email, phone number

    Contact information if willing to be alerted about future research

    Measured: enrollment in registry

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Feb 2024
  2. Study start3 Feb 2025
  3. Primary completion30 Sep 2025
  4. Study completion30 Sep 2025

Why it stopped: Sponsoring organization no longer desired to recruit/maintain registry

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
192 participants (actual)
Target duration
10 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT06275854
Sponsor's protocol ID
22265
Status last verified
Oct 2025
First submitted
22 Jan 2024
Last updated
14 Oct 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Cancer and Leukemia, run by Young Adult Survivors United at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 14 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Sponsoring organization no longer desired to recruit/maintain registry). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Anxiety (time frame: enrollment in registry, 6 months later, yearly until death). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Oct 2025; AzTrials last refreshed its copy on 7 Nov 2026.

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