Leveraging Technology to Achieve Equity for Men With Prostate Cancer on Androgen Deprivation Therapy

University of California San Francisco (UCSF)

Status

Completed

Conditions

Prostate Cancer

Treatments

Other: Survey Administration

Other: Text Messages

Other: STAND-T platform

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT05324098

215514

NCI-2022-02225 (Registry Identifier)

Details and patient eligibility

About

This clinical trial studies a digital platform, the supportive therapy in androgen deprivation (STAND-T), in achieving equity for men undergoing treatment with androgen deprivation therapy for prostate cancer. STAND-T is a digital platform that provides prostate health information, evidence-based materials and resources. STAND-T may help improve health, address symptoms, and promote equity in men with prostate cancer.

Full description

PRIMARY OBJECTIVE:

I. To assess study feasibility of the STAND-T program at the Helen Diller Family Comprehensive Cancer Center (HDFCCC) and Zuckerberg San Francisco General Hospital and Trauma Center (ZSFG) genitourinary (GU) medical, surgical, and radiation oncology practices.

SECONDARY OBJECTIVE:

I. To measure preliminary estimates of acceptability and usage of a digital platform, STAND-T.

EXPLORATORY OBJECTIVE:

I. To describe diet (e.g., fruit and vegetable intake), lifestyle (e.g., moderate to vigorous exercise, smoking status), clinical (symptoms e.g., fatigue), and health related quality of life (QoL) outcomes (e.g., sleep disturbance), physiologic measures (body mass index, BMI) at baseline and change in these metrics from baseline to 3 months post-intervention.

OUTLINE:

Patients review educational material and resources via online STAND-T platform. Patients also receive interactive text messages for 3 months.

After completion of study, patients are followed up at 3 months.

Enrollment

47 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age >18 years
Ability to understand study procedures and to comply with them for the entire length of the study
Ability of individual or legal guardian/representative to understand an informed consent document and the willingness to sign it
Adenocarcinoma of the prostate
Current or planned anti-androgen therapy (ADT) (oral or injection) with gonadotropin-releasing hormone (GnRH) antagonist or luteinizing hormone releasing hormone (LHRH) agonist
Life expectancy duration of 6 months or longer from date of study consent
Prior and concurrent radiation is allowed
Treatment with concurrent androgen signaling inhibitors is allowed
< 75 minutes/week of vigorous aerobic exercise based on Godin survey or < 2 days per week of vigorous activity

Exclusion criteria

Contraindication to any study-related procedure or assessment
Planned surgery/chemotherapy/immunotherapy/parp inhibitor treatment during the study period
Prior and concurrent investigational therapies
Unable to read/speak English
Unable to access the Internet
Has seen an exercise counselor in the past 6 months for prostate or cardiovascular health
Has seen a dietary counselor in the past 6 months for prostate or cardiovascular health