Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT04015609

Psychotherapy Intervention for Latinos With Advanced Cancer

Led by Memorial Sloan Kettering Cancer Center · Updated on 2025-10-02

190

Participants Needed

4

Research Sites

593 weeks

Total Duration

On this page

Sponsors

M

Memorial Sloan Kettering Cancer Center

Lead Sponsor

L

Lincoln Medical and Mental Health Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to adapt a counseling intervention called Meaning Centered Psychotherapy to make it culturally relevant for Latinos. Cancer affects patients and their loved ones. Latinos often experience greater challenges due to the cancer. However, few studies and interventions focus on Latinos. We are interested in understanding what affects Latino patients' quality of life, and how to improve it

CONDITIONS

Official Title

Psychotherapy Intervention for Latinos With Advanced Cancer

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with stage III or IV solid tumor cancer (self-reported for ICCAN patients)
  • Age 18 years or older
  • Self-reported Latino/a or Hispanic ethnicity
  • Fluent in spoken Spanish (either monolingual Spanish or bilingual Spanish and English)
  • For qualitative phase, enrolled in quantitative phase and completed questionnaire package
  • Scores above or below threshold on Distress Thermometer (≥4 or ≤3)
  • Willing and able to be interviewed in Spanish only
  • Agrees to audio recording of interviews
  • For provider feedback phase, mental health professionals with caseload of 5+ Latino cancer patients per month
  • Able to communicate and read in Spanish
  • Agrees to audio or video recording
  • For patient feedback phase, same criteria as above for advanced cancer, ethnicity, language, and agreement to audio recording
Not Eligible

You will not qualify if you...

  • Significant cognitive impairment (e.g., delirium or dementia) preventing informed consent or data collection
  • Major disabling medical or psychiatric conditions preventing consent, interview, or assessments (patients with well-controlled psychiatric disorders may participate)
  • For patient feedback phase, inability to understand consent or too ill to participate as determined by investigator or patient report

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Memorial Sloan Kettering Cancer Center

New York, New York, United States, 10065

Actively Recruiting

2

Ralph Lauren Center for Cancer Care and Prevention

New York, New York, United States

Actively Recruiting

3

Lincoln Medical and Mental Health Center

The Bronx, New York, United States

Actively Recruiting

4

Ponce Health Sciences University

Ponce, Puerto Rico, 00732

Actively Recruiting

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Research Team

R

Rosario Costas-Muniz, PhD

CONTACT

W

William Breitbart, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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