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Recruiting NCT05720546

Young Adult Infusion Space Experience Satisfaction Survey

— Observational Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Baseline Survey, Semi-structured interviews, Follow-up Survey.
Who it may be relevant to
Registry conditions: Cancer. Basic parameters: 18 years — 39 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Young Adult Infusion Space Survey: Comparing Experiences of Adolescents and Young Adults in Infusion Spaces at North Carolina Basnight Cancer Hospital

Overview

The purpose of this study is to compare the satisfaction of Adolescent and Young Adults (AYA) receiving treatment in two different infusion spaces at the North Carolina Basnight Cancer Hospital (NCBCH). A survey and semi-structured interviews will be administered to participants to compare the experience with the built environment, with mental health staff, and between outpatient infusion spaces at NCBCH.

Interventions

  • Other Baseline Survey
    A survey that measures participant satisfaction will be offered to participants during infusion at baseline.
  • Other Semi-structured interviews
    Semi-structured interviews will be conducted in the same infusion spaces.
  • Other Follow-up Survey
    A survey that measures participant satisfaction will be offered to participants during following infusion.

Primary outcome measures

  • General satisfaction [Time frame: Baseline (up to 1 month)]
Secondary outcome measures (3)
  • Satisfaction with the built environment [Time frame: Baseline (up to 1 month)]
  • Satisfaction with staff interaction [Time frame: Baseline (up to 1 month)]
  • Satisfaction with mental health [Time frame: Baseline (up to 1 month)]

Eligibility criteria

Inclusion criteria

  • Written informed consent obtained to participate in the study and HIPAA authorization for the release of personal health information.
  • Subjects are willing and able to comply with study procedures based on the judgment of the investigator or protocol designee.
  • Age 18-39 years old at enrollment.
  • Receiving treatment for a cancer diagnosis in Adult Infusion Center or the Adolescent and Young Adult Infusion Center
  • English speaking.

Exclusion criteria

  • Dementia, altered mental status, or any psychiatric condition as determined by the clinical or study team that would prohibit the understanding or rendering of informed consent.
  • Current incarceration.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • UNC Lineberger Comprehensive Cancer Center — Chapel Hill

Identifiers

NCT: NCT05720546 · LCCC2228

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗