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Behavioural Intervention

MamaLift Plus for Postpartum Depression (SuMMER Trial)

N/A
Waitlist Available
Led By Stan Kachnowski, PhD
Research Sponsored by Healthcare Innovation Technology Lab
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 9 week period

Summary

This trial is testing the effectiveness of the MamaLift Plus app for new mothers with mild to moderate post-partum depression. The app offers tools and support to help manage depression symptoms. Women aged 18 to 50 who have recently given birth are participating. The goal is to see if the app helps reduce their depression more than usual care alone.

Eligible Conditions
  • Postpartum Depression

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9 week period
This trial's timeline: 3 weeks for screening, Varies for treatment, and 9 week period for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
EPDS Score
EPDS Score improvement

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: MamaLift PlusExperimental Treatment1 Intervention
Principles of Cognitive Behavioral Therapy used to treat PPD with App
Group II: Digital Sham AppPlacebo Group1 Intervention
Content on general mental health and wellbeing topics delivered with sham App

Find a Location

Who is running the clinical trial?

Healthcare Innovation Technology LabLead Sponsor
4 Previous Clinical Trials
80 Total Patients Enrolled
Curio Digital Therapeutics, Inc.Industry Sponsor
1 Previous Clinical Trials
65 Total Patients Enrolled
Stan Kachnowski, PhDPrincipal InvestigatorHealthcare Innovation Technology Lab
1 Previous Clinical Trials
15 Total Patients Enrolled
~55 spots leftby Nov 2025
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