- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05588622
Meru Health Program for Cancer Patients With Depression and Anxiety
July 12, 2023 updated by: Nicholas Peiper, PhD, MPH, Meru Health, Inc.
Feasibility of a Therapist-Supported Digital Mental Health Intervention in Addressing Mental Health Symptoms Among People With Cancer: A Mixed Methods Study
The primary objective of this study is to evaluate clinical outcomes among people with cancer who participate in a 12-week therapist-supported digital mental health intervention (DMHI) called the Meru Health Program (MHP).
Study participants (N=20) will be referred to the MHP through the Cancer Support Community (CSC) Helpline and network of Gilda's Club locations.
The main outcomes will be depression symptoms, anxiety symptoms, health-related quality of life (HRQoL), intervention adherence, and intervention satisfaction.
The secondary objective will be to determine the acceptability of the screening and referral process from the CSC networks into the MHP.
Data pertaining to implementability will be collected from study participants, MHP clinicians, and CSC staff.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The goal of this single-arm intervention study is to test the feasibility of the Meru Health Program (MHP) in reducing symptoms of depression and anxiety among 20 people with cancer referred from the Cancer Support Community (CSC).
The MHP is a 12-week digital mental health intervention delivered via a smartphone app.
The intervention focuses on cognitive behavioral techniques and mindfulness skills with the aim of improving mental health symptoms.
The platform provides informational videos, skills practices, group discussion, and messaging with a licensed clinician employed by Meru Health.
The licensed clinician supports patients as needed and reviews engagement logs within the app.
As part of the intervention, depression and anxiety symptoms are measured on a biweekly basis over 12 weeks.
For this study, self-reported surveys will be administered at baseline, week 12, and 2-months post-treatment to measure health-related quality of life and intervention satisfaction.
In-depth interviews will be conducted with patients.
Two focus groups will be conducted with MHP clinicians and CSC navigators to understand barriers and facilitators to the screening processes and intervention delivery.
Study Type
Interventional
Enrollment (Actual)
22
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Colorado
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Denver, Colorado, United States, 80014
- Online Digital Mental Health Clinic
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Positive screen (score >= 3 out of 8) on the anxiety or depression subscale of the CSS 15+ Questionnaire
- PHQ-9 and/or GAD-7 score >= 5 at clinical intake
- Willing to commit to the Meru Health Program if selected
- Proficient in the English language
- At least 18 years of age at the time of enrollment
- Has a valid mailing address
- Owns 1 of the 3 past versions of an Apple or Android mobile phone operating system
- Currently in active cancer treatment at the time of enrollment
Exclusion Criteria:
- Active suicide intent with plan to act
- Substance use disorder in the past 3 months
- Lifetime bipolar disorder
- Lifetime psychotic disorder
- Currently pregnant
- Less than 3 months postpartum
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment Group
This single-arm study will enroll all 20 participants in the Meru Health Program.
|
The Meru Health Program is a 12-week, evidence-based, smartphone-delivered, therapist-supported digital mental health intervention with as-needed psychiatrist oversight.
Enrolled participants work through the program with a cohort of peers similarly affected by depression, with whom they can engage in confidential, anonymous, voluntary group chats overseen by a licensed clinical therapist.
The MHP incorporates a continuous care model including daily interaction with a dedicated clinician, several evidence-based treatment components such as cognitive behavioral therapy (CBT), behavioral activation therapy, and mindfulness meditation (MM), as well as promising newer types of depression treatments such as HRVB, nutritional psychiatry, and sleep training.
Practices are introduced to weekly topics via video lessons that are reinforced via CBT practices, meditations, and biofeedback sessions and therapist messaging.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in PHQ-9 Scores
Time Frame: Baseline, Week 12, and 2 Month Follow-Up time points
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9-item questionnaire to measure depression symptoms
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Baseline, Week 12, and 2 Month Follow-Up time points
|
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Change in GAD-7 Scores
Time Frame: Baseline, Week 12, and 2 Month Follow-Up time points
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7-item questionnaire to measure anxiety symptoms
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Baseline, Week 12, and 2 Month Follow-Up time points
|
|
Change in Eurohis-QOL-8 Scores
Time Frame: Baseline, Week 12, and 2 Month Follow-Up time points
|
8-item Quality of Life questionnaire.
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Baseline, Week 12, and 2 Month Follow-Up time points
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Change in CSS 15+ Scores
Time Frame: Baseline and Week 12 time points
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15-item questionnaire to measure psychological distress experiencing and receiving treatment for cancer.
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Baseline and Week 12 time points
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Burnout Scores
Time Frame: Baseline, Week 12, and 2 Month Follow-Up
|
A single-item questionnaire to address worker stress and burnout.
|
Baseline, Week 12, and 2 Month Follow-Up
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 6, 2022
Primary Completion (Actual)
June 9, 2023
Study Completion (Actual)
July 1, 2023
Study Registration Dates
First Submitted
October 13, 2022
First Submitted That Met QC Criteria
October 18, 2022
First Posted (Actual)
October 20, 2022
Study Record Updates
Last Update Posted (Actual)
July 13, 2023
Last Update Submitted That Met QC Criteria
July 12, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 22-MERU-117
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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