Friendly video chats may lift depression in older adults
NCT ID NCT05611996
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tested whether support from a peer mentor through video chats and texts could help reduce depression in older adults, especially those with low income or from ethnic minority groups. 34 participants aged 50 and older with mild depression took part in 8 weekly video chats and received supportive texts. The main goal was to see if this approach was practical and well-received.
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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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34 people
The number who actually took part.
- Started
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Dec 2022
- Finished
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Jan 2025
- 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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50 years and older
- 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. 50 years and older 2. PHQ-9 score \> 5, 3. on the same antidepressant dose for at least 3 months 4. if receiving psychotherapy, frequency is at most once a month 5. able to communicate in English 6. able to give informed consent. Exclusion Criteria: 1. meet diagnostic criteria for mania or hypomania 2. active suicidal ideation 3. meet diagnostic criteria for psychotic syndrome 4. meet diagnostic criteria for substance abuse or dependence 5. cognitive impairment, with a score on the Short Blessed Test \> 9.
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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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Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
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Other studies related to the condition(s) this trial covers.
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