A tool for managing stress and improving quality of life in cancer patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of My Wellbeing Guide, a psychosocial eHealth intervention designed to reduce depressive symptoms in cancer patients. The intervention employs cognitive behavioral therapy strategies delivered through an online application over a 7-week period, featuring animated videos, interactive activities, and written content. Participants will be randomized into either the intervention or a control group, with assessments conducted at baseline, post-intervention, and at 6- and 12-month follow-ups. The study aims to address the high prevalence of depression among cancer patients and improve their overall quality of life.

Why it matters

Who can join: the full rules

Inclusion Criteria:

a) having been reached out to by the study team for recruitment; (b) planned treatment and follow-up within the NM or UHealth healthcare system; (c) ≥ 18 years of age; (d) medical chart confirmed diagnosis of a solid or hematological malignancy; (e) elevated depressive symptoms on the PROMIS CAT (score \> or = 55) within the last 3 months; (f) access to the internet; (g) willingness to be randomized; (h) able to read English or Spanish; (i) patients must have signed informed consent prior to registration on study

Exclusion Criteria:

Note: The investigators will not include any vulnerable populations in this study.

Where it's running

• Northwestern University
  Chicago, Illinois, United States Recruiting

Study contacts

• Principal investigator: Betina Yanez, PhD — Northwestern University
• Study coordinator: Ro Mercer, BS
• Email: ro.mercer@northwestern.edu
• Phone: 312-503-3943

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.