Behavioral Activation for Depression in Older Adults in Primary Care
Official title: Behavioral Activation for the Treatment of Depression in Older Adults: A Randomised Controlled Multicenter Trial in Primary Care (DepActive)
Run by Uppsala University · NCT06284889 · Data updated 2026-11-12
A telephone-based behavioral activation program is being tested to see if it can reduce depressive symptoms in people 65 and older who live in Sweden and visit primary care.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 65 Years and up |
| Sex | All |
| Enrollment | 81 (estimated) |
| Sponsor | Uppsala University Academic / other |
| Locations | 2 sites (Uppsala, Uppland and 1 other locations) |
| Status | Recruiting |
| Started | March 4, 2024 |
| Main results expected | November 15, 2026 |
| Study ends | November 15, 2026 |
| Registry record updated | October 15, 2026 |
| Trial ID | NCT06284889 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Community-dwelling adults aged 65 and older with current major or sub-threshold depressive episodes, fluent in Swedish, with telephone access, and willing to participate in a randomized trial.
✕Probably not a fit
Individuals with severe depression, high suicide risk, active psychosis, substance use disorder, certain neurocognitive disorders, or ongoing psychotherapy may not benefit from this intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized multicenter study in Sweden tests a telephone-delivered behavioral activation intervention against treatment as usual for adults 65 and older with major or sub-threshold depression. The goal is to determine effects on depressive symptoms, depression diagnosis, anxiety, and quality of life. Participants will be randomly assigned to start the behavioral activation treatment or continue standard care, with activities aimed at increasing meaningful and enjoyable behaviors. The intervention builds on prior pilot work showing that telephone support can reduce depressive symptoms and maintain gains over six months. Recruitment targets 250 participants across participating centers under the DepActive framework.
Why it matters
Potential benefit: If successful, participants may experience fewer depressive symptoms and improved quality of life through more engaging daily activities without needing in-person therapy.
How similar studies have gone: Prior pilot work and related telepsychology research suggest behavioral activation can reduce depression symptoms when delivered remotely, supporting potential benefit in this setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants should fulfill criteria for current major depressive episode or sub-threshold depressive episode. * Eligible participants should be 65 years or older, should be fluent in spoken and written Swedish to understand the treatment materials, have access to telephone, and be interested in participating in the trial. Exclusion Criteria: * Severe depression, elevated suicide risk, current substance use disorder, current or previous manic or hypomanic episodes, current psychotic disorder, and current diagnosis of minor or major neurocognitive disorder or suspected neurocognitive disorder with \< 24 points on the Mini Mental State Examination number 3, MMSE-NR3. * ongoing psychotherapy
Where it's running
-
Dept Public Health and caring sciences, Uppsala university
Uppsala, Sweden Recruiting -
Uppsala university
Uppsala, Uppland, Sweden Not yet recruiting
Study contacts
- Principal investigator: Mattias Damberg, MD, Associate Professor — Uppsala university, Dept. Public Care and Health Sciences
- Study coordinator: Mattias Damberg, MD
- Email: mattias.damberg@uu.se
- Phone: +46739480910
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Smartphone-supported single-session psychotherapy for postpartum depression
A single online therapy session plus four weeks of app-based support is being tested to see if it reduces depressive symptoms in postpartum women compared with a waitlist.
-
Mindful Smartphone Use: A Mindfulness-Based Program for Teens with Sleep and Mood Challenges
This study tests Mindwire, a mindfulness-based program, to see if it helps teens with problematic phone use who also have depression or anxiety.
-
Tele-based wellbeing centres for women's mental health in Bangladesh
A randomized trial tests whether tele-counselling for depression and anxiety in Bangladeshi women is as effective as in-person counselling.
-
Remote monitoring for adults with depression using ThIA Suivi
This study tests whether adding the ThIA Suivi remote monitoring tool to usual psychiatric care helps adults with depression feel more improved after 3 months compared with standard care alone.
-
HBOT to see if it helps cognition and well‑being in first responders with prior brain injury
This study tests whether 40 hyperbaric oxygen therapy sessions can improve thinking skills and post-concussion symptoms in current or former first responders with a history of brain injury.
-
Focused ultrasound for mood and anxiety disorders
This study tests whether repeated low-intensity focused ultrasound using the ATTN201 device can help people with subsyndromal to moderate depression, anxiety, or OCD.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.