Can a text message ease depression? new study tests digital therapy for young adults
NCT ID NCT04948268
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested an 8-week text messaging program for young adults (ages 18-25) with depression or anxiety who do not want in-person therapy. Some participants got personalized messages tailored by a computer, while others got standard messages or weekly tips. The goal was to see if this approach could reduce distress and keep people engaged. The study involved 120 participants and was completed in the United States.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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120 people
The number who actually took part.
- Started
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Oct 2023
- Finished
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Oct 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 25 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Ages 18 to 25 \*The age to provide consent in Nebraska is 19. Individuals recruited from the state of Nebraska must be 19 or older. 2. A positive screen on an MHA screen for depression (Patient Health Questionnaire - 9 \[PHQ-9\]) or anxiety (Generalized Anxiety Disorder - 7 \[GAD-7\]); 3. Resident of the United States. 4. Owns a smartphone Exclusion Criteria: 1. Current treatment with psychotherapy or psychiatric medication management; 2. Seeking or plans to seek traditional mental health treatment (psychotherapy or psychiatric medication management) in next 8 weeks; 3. Serious mental illness for which intervention would be contraindicated (e.g., psychotic disorder, manic episode, etc.) 4. Severe suicidality (i.e., experiencing suicidal ideation with a plan and intent to act); 5. English insufficient to engage in design activities.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Northwestern University
Chicago, Illinois, 60611, United States
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Other studies related to the condition(s) this trial covers.
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