300,000 people join digital mental health experiment
NCT ID NCT07183085
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study will observe 300,000 adults using a digital mental health program that includes physical activity, sleep tips, and mindfulness. Researchers want to see if people engage with the program and if their anxiety and depression symptoms improve. It is an observational study, meaning it collects data without assigning treatments, so it can show patterns but not prove what works.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Digital mental health program (personalized exercises, sleep hygiene, mindfulness)
- What this could lead to
- If successful, this could show that digital programs are a scalable way to improve mental health for many people.
- What could go wrong
- This is an observational study, not a controlled trial, so it cannot prove cause and effect. Results may not apply to everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 300,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Sep 2025
- Expected to finish
-
Dec 2035
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This program is designed to support individuals experiencing mental distress to improve overall wellbeing and mood symptom improvement.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 18 years old and above; * able to understand study procedures and willing to provide informed consent. Exclusion Criteria: * suicidal ideation with plan in the past 6 months; * self-reported scores of the Patient Health questionnaire-9 (PHQ-9) above 19; * suffering from any of the following mental health conditions: Schizophrenia, Bipolar Disorder, Alcohol Use Disorder, Substance Use Disorder, Eating Disorder, Post-Traumatic Stress Disorder.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Mental distress are added.
By submitting, you agree to our Terms of use
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Sword Health
New York, New York, 10016, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.