Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06960993

Mosaic Trial for Stem Cell Transplant Recipients

Led by Northwestern University · Updated on 2025-07-18

356

Participants Needed

3

Research Sites

248 weeks

Total Duration

On this page

Sponsors

N

Northwestern University

Lead Sponsor

G

Georgetown University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if using an intervention website (Mosaic) improves selected patient-reported outcomes in adult blood cancer patients undergoing allogeneic or autologous stem cell transplant, compared to using an educational website (control group). Patients will be recruited prior to their scheduled transplant, then randomized to use one of these two study websites throughout the study. They will complete five assessments during the study: one before transplant (baseline) and four after transplant (2, 4, 6, and 8 month follow-ups). The main questions this trial aims to answer are: 1. Compared to patients using the control group website, do patients using the intervention website report greater improvements in general psychological distress, cancer treatment-related distress, physical symptoms, and health-related quality of life? 2. Are these benefits at least partially explained by improvements in perceived preparedness, self-efficacy, and approach coping and/or reductions in avoidant coping and perceived stress? 3. Do some patients benefit more from using the intervention website than others? Specifically, we will examine whether patients' primary language (English/Spanish) and their initial psychological distress are related to the benefit they get from using the intervention website. We will also explore effects of sex, race, ethnicity, and transplant type.

CONDITIONS

Official Title

Mosaic Trial for Stem Cell Transplant Recipients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with a hematologic cancer according to medical records
  • Scheduled for or preparing for scheduling of an allogeneic or autologous stem cell transplant at one of our study sites
  • Aged 18 or older (no upper limit)
  • English or Spanish proficient
  • Interested in using a website to learn about stem cell transplant
  • Ability to understand and willingness to sign an informed consent document and comply with all study procedures
Not Eligible

You will not qualify if you...

  • Currently participating in a behavioral intervention targeting distress, health-related quality of life, or symptoms
  • Undergoing the first in a planned tandem stem cell transplant
  • Unable to provide meaningful consent (severe cognitive impairment or language difficulties)

AI-Screening

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Trial Site Locations

Total: 3 locations

1

Georgetown University School of Medicine

Washington D.C., District of Columbia, United States, 20057

Actively Recruiting

2

Northwestern University Feinberg School of Medicine

Chicago, Illinois, United States, 60611

Actively Recruiting

3

Hackensack Meridian Health

Nutley, New Jersey, United States, 07110

Actively Recruiting

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Research Team

C

Christine Rini, PhD

CONTACT

S

Sonia Zavala

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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