Actively Recruiting
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
Eligibility Criteria
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
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
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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