SCIPI Implementation and Evaluation: A Multi-site Proof-of-Concept Pilot Trial

Part of paid clinical trials in San Antonio, Texas.

Sponsor
The University of Texas Health Science Center at San Antonio
Study ID
NCT07280897
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • SCIPI — BEHAVIORAL
    SCIPI (Support, Communication, and Information Program for Prostate Cancer - Interactive) is a web-based supportive care program delivered through the Epic MyChart system. The program provides tailored educational materials, skills training, and interactive tools to support informed treatment decision-making for patients with localized prostate cancer.

Study Details

This study will test a web-based supportive care program called the Support, Communication, and Information Program for Prostate Cancer - Interactive (SCIPI). SCIPI provides men with localized prostate cancer and their families with easy-to-understand information, tools to prepare for discussions with their doctors, and opportunities for social support. The purpose of this pilot study is to determine whether it is feasible to integrate SCIPI in prostate cancer clinical care via the electronic medical record and whether SCIPI may improve patients' confidence in making treatment decisions and their overall quality of life compared with usual care. The study will include patients who are newly diagnosed with prostate cancer. Participants will be randomly assigned to use SCIPI or to receive usual care, and information will be collected over time about their experiences, decision-making, and quality of life.

Key Dates

Start date
Oct 1, 2026
Status verified
Dec 2025
Primary completion
Sep 29, 2029
Completion
Sep 29, 2029

Study Design

Enrollment
200 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: SCIPI
    Participants will receive SCIPI, a web-based supportive care program delivered through the Epic MyChart system, in addition to usual care.
  • No Intervention: Usual Care
    Participants will receive usual care provided at their study site.

Primary Outcome Measure

Satisfaction with Decision (SWD) [ Time Frame: 3-month follow-up (T2) and 6-month follow-up (T3) ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
The University of Texas Health Science Center at San Antonio School of NursingSan AntonioTexas78229
Cheongin Im, Postdoctoral Research Fellow, PhD, MSN
[email protected]
210-567-5120
Lixin Song, Vice Dean for Research and Scholarship Professor, PhD
[email protected]
210-450-8917

Find similar trials in San Antonio, TX

By condition
Prostate cancer
By specialty
OncologyProstate oncologyMen's healthUrology
By research site
The University of Texas Health Science Center at San Antonio School of Nursing· San Antonio, TX

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