Young Adult Infusion Space Experience Satisfaction Survey

NCT ID: NCT05720546

Last Updated: 2025-10-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-02-20

Study Completion Date

2026-08-31

Brief Summary

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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.

Detailed Description

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Conditions

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Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Outpatient treatment center

Subjects received an infusion in an outpatient infusion center.

Baseline Survey

Intervention Type OTHER

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

Semi-structured interviews

Intervention Type OTHER

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

Follow-up Survey

Intervention Type OTHER

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

Inpatient Infusion Center

Subjects received an infusion in an inpatient infusion center.

Baseline Survey

Intervention Type OTHER

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

Semi-structured interviews

Intervention Type OTHER

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

Follow-up Survey

Intervention Type OTHER

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

Interventions

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Baseline Survey

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

Intervention Type OTHER

Semi-structured interviews

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

Intervention Type OTHER

Follow-up Survey

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

1. 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.
2. Current incarceration.
Minimum Eligible Age

18 Years

Maximum Eligible Age

39 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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UNC Lineberger Comprehensive Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jacob Stein

Role: PRINCIPAL_INVESTIGATOR

UNC Lineberger Comprehensive Cancer Center

Locations

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UNC Lineberger Comprehensive Cancer Center

Chapel Hill, North Carolina, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Daniel Kleissler

Role: CONTACT

919-928-6231

Facility Contacts

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Daniel Kleissler

Role: primary

Related Links

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http://unclineberger.org/patientcare/clinical-trials/clinical-trials

University of North Carolina Lineberger Comprehensive Cancer Center Clinical Trials

Other Identifiers

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LCCC2228

Identifier Type: -

Identifier Source: org_study_id

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