NCT05720546

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
4mo left

Started Feb 2023

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress91%
Feb 2023Aug 2026

First Submitted

Initial submission to the registry

January 31, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

February 9, 2023

Completed
11 days until next milestone

Study Start

First participant enrolled

February 20, 2023

Completed
3.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2026

Last Updated

October 24, 2025

Status Verified

October 1, 2025

Enrollment Period

3.5 years

First QC Date

January 31, 2023

Last Update Submit

October 22, 2025

Conditions

Keywords

Adolescentsurvey

Outcome Measures

Primary Outcomes (1)

  • General satisfaction

    General satisfaction will be measured with participants' responses to satisfaction surveys that will be administered in specific infusion spaces. Responses are rated on a Likert scale from 0 to 4. Scores will be summarized using frequency tables and percentages.

    Baseline (up to 1 month)

Secondary Outcomes (3)

  • Satisfaction with the built environment

    Baseline (up to 1 month)

  • Satisfaction with staff interaction

    Baseline (up to 1 month)

  • Satisfaction with mental health

    Baseline (up to 1 month)

Study Arms (2)

Outpatient treatment center

Subjects received an infusion in an outpatient infusion center.

Other: Baseline SurveyOther: Semi-structured interviewsOther: Follow-up Survey

Inpatient Infusion Center

Subjects received an infusion in an inpatient infusion center.

Other: Baseline SurveyOther: Semi-structured interviewsOther: Follow-up Survey

Interventions

A survey that measures participant satisfaction will be offered to participants during infusion at baseline.

Inpatient Infusion CenterOutpatient treatment center

Semi-structured interviews will be conducted in the same infusion spaces.

Inpatient Infusion CenterOutpatient treatment center

A survey that measures participant satisfaction will be offered to participants during following infusion.

Inpatient Infusion CenterOutpatient treatment center

Eligibility Criteria

Age18 Years - 39 Years
Sexall
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

A subject with a cancer diagnosis and receiving infusion in the study site

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UNC Lineberger Comprehensive Cancer Center

Chapel Hill, North Carolina, 27514, United States

RECRUITING

Related Links

MeSH Terms

Conditions

Neoplasms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Jacob Stein

    UNC Lineberger Comprehensive Cancer Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 31, 2023

First Posted

February 9, 2023

Study Start

February 20, 2023

Primary Completion (Estimated)

August 31, 2026

Study Completion (Estimated)

August 31, 2026

Last Updated

October 24, 2025

Record last verified: 2025-10

Locations