My Wellbeing Guide for Anxiety and Depression in Cancer Patients
My Wellbeing Guide: A Novel Tool for Managing Stress and Improving Quality of Life
Recruiting
N/AInterventional Study
CancerAnxietyDepressive Symptoms
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
6,516 (estimated)
Sponsor
Northwestern University · Other
Who this trial is looking for
This trial is looking for cancer patients over 18 who have symptoms of depression. Participating includes using an online program that offers resources for managing stress over 7 weeks and completing some follow-up assessments.
Are You a Good Fit for This Trial?
You may be able to join if
I have been contacted by the study team to take part.
I am 18 years or older.
I have a confirmed diagnosis of cancer.
I have elevated depressive symptoms in the last 3 months.
I have access to the internet.
I can read English or Spanish.
I am willing to be part of a random selection process.
I will sign an informed consent before joining the study.
You may not be able to join if
I am part of a vulnerable population.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
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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 int…
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.
Trial Locations
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Eligibility Criteria
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 …
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.
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