Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05369429

My Wellbeing Guide: A Novel Tool for Managing Stress and Improving Quality of Life

Led by Northwestern University · Updated on 2026-04-20

6516

Participants Needed

1

Research Sites

182 weeks

Total Duration

On this page

Sponsors

N

Northwestern University

Lead Sponsor

U

University of Miami

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to examine the implementation and effectiveness of the psychosocial eHealth intervention, My Wellbeing Guide, on the proposed primary outcome, depressive symptoms, in patients diagnosed with cancer who receive care at Northwestern Medicine and the University of Miami Health System. Eligible patients will be directly contacted by the study team for recruitment. The intervention includes cognitive behavioral therapy management strategies for health-related stress in the form of animated videos, interactive activities, and written content. The intervention will be delivered via an online application over an 7-week period. Intervention participants will also complete four assessments: baseline (at the beginning of the research study), post-intervention (7 weeks after baseline), a 6-month follow-up, and a 12-month follow up. Participants are randomized into either an intervention application (described above) or a control application (which will provide links to helpful resources for patients with cancer, such as the contact information for cancer support services at Northwestern University and the University of Miami, and the link to the National Cancer Institute website, and the American Cancer Society website.) Control participants will also complete four assessments: baseline (at the beginning of the research study), post-intervention (7 weeks after baseline), a 6-month follow-up, and a 12-month follow up.

CONDITIONS

Official Title

My Wellbeing Guide: A Novel Tool for Managing Stress and Improving Quality of Life

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have been contacted by the study team for recruitment
  • Planned treatment and follow-up within the Northwestern Medicine or University of Miami Health System
  • 18 years of age or older
  • Medical chart confirmed diagnosis of a solid or hematological malignancy
  • Elevated depressive symptoms on the PROMIS CAT (score ≥ 55) within the last 3 months
  • Access to the internet
  • Willingness to be randomized
  • Able to read English or Spanish
  • Signed informed consent prior to registration on study
Not Eligible

You will not qualify if you...

  • Vulnerable populations are not included in this study

AI-Screening

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Trial Site Locations

Total: 1 location

1

Northwestern University

Chicago, Illinois, United States, 60611

Actively Recruiting

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Research Team

R

Ro Mercer, BS

CONTACT

B

Betina Yanez, PhD

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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