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Virtual Testis Cancer Lay Support and Survivorship Aim 2 (VITALSS)

UNC Lineberger Comprehensive Cancer Center logo

UNC Lineberger Comprehensive Cancer Center

Status

Begins enrollment this month

Conditions

Testicular Cancer
Testis Cancer

Treatments

Behavioral: Patient educational material
Behavioral: Virtual support

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT06702592
LCCC2418 AIM2

Details and patient eligibility

About

This study examines how virtual support can enhance well-being and survivorship in men with testicular cancer. Participants in North Carolina will be randomized into two groups: one with access to a virtual support platform and the other with access to patient educational materials only. After six months, the emotional well-being, self-efficacy, financial toxicity, and quality of life of both groups will be compared at 3 months and 6 months after baseline assessments.

Enrollment

360 estimated patients

Sex

Male

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Men within 5 years of their initial diagnosis of germ cell testicular cancer.
  • The subject is willing and able to comply with study procedures based on the judgment of the investigator.
  • Adults aged 18-95 years old.
  • Electronic informed consent was obtained to participate in the study.

Exclusion criteria

  • Woman gender
  • Non-English speaking
  • Unwilling or unable to complete informed consent.
  • On active treatment for another cancer.
  • Actively receiving chemotherapy, radiation, or surgery for testicular cancer.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

360 participants in 2 patient groups

Virtual support
Experimental group
Description:
Participants will have access to the virtual support platform.
Treatment:
Behavioral: Virtual support
Patient educational material
Other group
Description:
Participants will have access to patient educational material only.
Treatment:
Behavioral: Patient educational material

Trial contacts and locations

1

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Central trial contact

Deborah S Usinger; Taylor J Greene

Data sourced from clinicaltrials.gov

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