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OpenTrials
Completed

NCT Number: NCT06003361

Rise Study for Depression

This study will examine the efficacy of digital CBT versus waitlist in improving symptoms for adults with Major Depressive Disorder.

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Key information

Age range

22 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Big Health Inc.

San Francisco, California, 94108, United States

About this study

This study aims to examine the effectiveness of app-based digital CBT in individuals with a diagnosis of Major Depressive Disorder. The primary outcomes are depression symptom reduction and engagement with fulfilling activities after 5 weeks.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged ≥22 years old
  • Score ≥10 and <20 on the 8-item Patient Health Questionnaire (PHQ-8)
  • Diagnosis of Major Depression
  • Current resident of the USA
  • Oral and written fluency in English
  • Regular access to the internet via a mobile or tablet device using Android (5 or higher) or iOS (13 or higher)
  • Participant is able and willing to comply with protocol requirements, has been informed of the nature of the study, and has signed the IRB-approved informed consent form

Exclusion criteria

  • Must not be currently receiving or be expecting to start therapy for depression, anxiety, or sleep during study participation, or have received cognitive behavioral therapy for depression, anxiety, or sleep in the past 12-months
  • If on psychotropic medication, this must be stable for at least 60 days
  • Past or present psychosis, schizophrenia, or bipolar disorder
  • Moderate or greater suicide risk
  • Treatment-resistant depression
  • Hearing or vision impairment that prevents effective use of the audio-visual content of digital CBT or psychoeducation
  • Intellectual disability or any Neurocognitive or Neurodevelopmental disorder that would prevent participants from following study procedures
  • Any condition that the investigator believes would make participation in the study not in the best interest of the subject or would preclude successful completion of study activities
  • Other exclusion criteria may apply

Treatment and study plan

digital CBT

Device

An app-based intervention based on principles from cognitive behavioral therapy for depression.

Waitlist

Other

Participants will wait for 5 weeks prior to receiving the intervention

Primary outcomes

  1. Patient Health Questionnaire (PHQ-8)

    Time frame: 5 weeks post-randomization

    Validated questionnaire; an 8-item scale with total scores between 0 and 24 where higher scores indicate greater severity

  2. Environmental Reward Observation Scale (EROS)

    Time frame: 5 weeks post-randomization

    A validated 10 item scale with total scores between 10 and 40 where higher scores indicate greater engagement with rewarding or fulfilling life activities

Secondary outcomes

  1. Patient Health Questionnaire (PHQ-8)

    Time frame: 10 weeks post-randomization

    Validated questionnaire; an 8-item scale with total scores between 0 and 24 where higher scores indicate greater severity

  2. Montgomery-Åsberg Depression Rating Scale (MADRS)

    Time frame: 5 and 10 weeks post-randomization

    A validated 10 item observer-rated scale with total scores between 0 and 60 where higher scores indicate greater severity

  3. World Health Organization 5-item Wellbeing Index (WHO-5)

    Time frame: Weeks 5 and 10 post-randomization

    Validated questionnaire; a 5-item scale with raw total scores between 0 and 25 where higher scores indicate greater wellbeing

  4. Environmental Reward Observation Scale (EROS)

    Time frame: 10 weeks post-randomization

    A validated 10 item scale with total scores between 10 and 40 where higher scores indicate greater engagement with rewarding or fulfilling life activities

Sponsors and collaborators

Lead sponsor

Big Health Inc.

Industry

Registry information

Official study title

Randomized Controlled Trial of a Digital Cognitive Behavioral Therapy Program for Major Depression in Adults

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Aug 21, 2023
Registry last updated
Jan 17, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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