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Behavioral Activation for the Treatment of Depression in Older Adults - Trial NCT06284889

Access comprehensive clinical trial information for NCT06284889 through Pure Global AI's free database. This phase not specified trial is sponsored by Uppsala University and is currently Not yet recruiting. The study focuses on Depression. Target enrollment is 250 participants.

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NCT06284889
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behavioral
Trial Details
ClinicalTrials.gov โ€ข NCT06284889
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Behavioral Activation for the Treatment of Depression in Older Adults
Behavioral Activation for the Treatment of Depression in Older Adults: A Randomised Controlled Multicenter Trial in Primary Care (DepActive)

Study Focus

Depression

Behavioural activation

Interventional

behavioral

Sponsor & Location

Uppsala University

Uppsala, Sweden

Timeline & Enrollment

N/A

Mar 04, 2024

Dec 31, 2028

250 participants

Primary Outcome

Change from baseline in depressive symptoms using the Montgomery-Asberg Depression Rating Scale, MADRS-S

Summary

Depression affects between 5-15% of adults โ‰ฅ 65 years in Sweden. Depression in older adults
 reduces functional ability and quality of life, and increases the risk for morbidity,
 loneliness, and suicide. Psychological treatment is recommended as a first-line treatment for
 depression, which about 3% of older adults with depression in Sweden report receiving. One
 effective psychological treatment is behavioral activation, which reduces depressive symptoms
 by increasing enjoyable, meaningful and important activities, for example exercise and social
 activities. The research group conducted a pilot study of telephone based behavioral
 activation for isolated older adults with depression during the COVID-19 pandemic. The
 intervention consisted of four telephone calls, and the results showed a significant decrease
 in depressive symptoms, with maintained effects for six months.
 
 250 individuals will participate in the study. Half of the participants will be randomised to
 start the intervention immediately, while the other half of the participants will be
 randomized to a control group receiving treatment as usual at their respective primary care
 center. Participants will be asked to fill in questionnaires before, after treatment.
 Questionnaires will also be sent 3- and 6 months after treatment to follow up on the results.
 Patients will be asked to wear an accelerometer for 5-7 days to record their activity level
 at baseline, post-intervention and after 3-months. A smaller group of participants (10-15)
 will be asked to participate in a more detailed interview about how they experienced the
 treatment.

ICD-10 Classifications

Depressive episode
Other depressive episodes
Recurrent depressive disorder
Recurrent depressive disorder, unspecified
Post-schizophrenic depression

Data Source

ClinicalTrials.gov

NCT06284889

Non-Device Trial