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Behavioral Intervention

PRISM Intervention for Breast Cancer (PRISM Trial)

N/A
Recruiting
Led By Gabrielle Rocque, MD, MSPH
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Women undergoing neoadjuvant chemotherapy with early-stage breast cancer
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 years
Awards & highlights

PRISM Trial Summary

This trial tests a program called PRISM that helps people, particularly adolescents and young adults with cancer, to build resilience through coaching sessions focused on stress management, goal-setting, and positive thinking. Previous studies

Who is the study for?
This trial is for women receiving initial chemotherapy for early-stage breast cancer or treatment for metastatic breast cancer. It aims to help those who may benefit from building resilience and managing stress during their cancer journey, including marginalized communities.Check my eligibility
What is being tested?
The PRISM program is being tested, which involves skills-based coaching to improve resilience through stress management, goal-setting, and positive reframing. The intervention has shown promise in other settings and will be tailored for adult women with breast cancer.See study design
What are the potential side effects?
Since PRISM focuses on psychological support rather than medication, traditional side effects are not a concern. However, participants might experience emotional discomfort as they engage with the intervention's activities.

PRISM Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am a woman receiving initial chemotherapy for early-stage breast cancer.

PRISM Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 5 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Promoting Resilience in Women with Breast Cancer

PRISM Trial Design

1Treatment groups
Experimental Treatment
Group I: PRISM InterventionExperimental Treatment1 Intervention
This single-arm pilot study will (1) test feasibility, acceptability, and appropriateness of the PRISM intervention in individuals with breast cancer, (2) elicit patient perspectives on elements for future adaptation or expansion to meet the unique needs of women with breast cancer, (3) assess trajectory of patient-reported outcomes and biological measures of stress for patients with breast cancer receiving the PRISM intervention.

Find a Location

Who is running the clinical trial?

University of Alabama at BirminghamLead Sponsor
1,590 Previous Clinical Trials
2,281,422 Total Patients Enrolled
31 Trials studying Breast Cancer
4,451 Patients Enrolled for Breast Cancer
Gabrielle Rocque, MD, MSPHPrincipal InvestigatorThe University of Alabama at Birmingham

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the collective count of individuals actively involved in this research trial?

"Indeed, the information on clinicaltrials.gov indicates that this investigation is currently enrolling participants. The trial was initially listed on January 24th, 2024, and last modified on February 22nd, 2024. They aim to recruit a total of 40 patients from one designated site."

Answered by AI

Are new patients still eligible to participate in this ongoing clinical trial?

"Indeed, data from clinicaltrials.gov indicates that this investigation is actively seeking participants. The trial was first listed on January 24th, 2024 and last revised on February 22nd, 2024. It aims to recruit a total of 40 patients from one designated site."

Answered by AI
~27 spots leftby Dec 2025