Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
ID06415838

Behavioral Activation for the Prevention and Treatment of Depression in Older Adults in a Municipal Context: a Randomized Controlled Trial

Led by Sormland County Council, Sweden · Updated on 2024-12-16

160

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

Sponsors

S

Sormland County Council, Sweden

Lead Sponsor

E

Eskilstuna municipality

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating a brief psychological treatment called Behavioral Activation (BA) to prevent and treat depression in adults aged 65 and older within a municipal care setting in Sweden. Depression is common among older adults and affects quality of life and daily functioning. This trial aims to understand whether BA can improve depressive and anxiety symptoms, self-rated activation, functional ability, loneliness, self-efficacy, mental wellbeing, quality of life, and reduce the need for community care services. The study also explores experiences of both patients and therapists involved in the BA treatment. Participants will continue their usual care, and half will be randomly assigned to receive a five-session BA treatment over two months, delivered face-to-face in their homes by social workers. The BA sessions start weekly for four weeks, followed by a booster session four weeks later. The other half will receive care as usual without the BA intervention. This design allows comparison between BA plus usual care and usual care alone. Participants will complete questionnaires at the start, after two months, and at 3, 6, and 12 months to assess outcomes including depressive symptoms measured with the Montgomery-Åsberg Depression Rating Scale. Additional evaluations include anxiety, disability, loneliness, self-efficacy, mental wellbeing, quality of life, and community care needs. The total participation spans one year, with data collected to understand both short- and long-term effects of the BA treatment.

CONDITIONS

Brief Title

Behavioral Activation for the Prevention and Treatment of Depression in Older Adults in a Municipal Context

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 65 years or older
  • Score of 5 points or above on the Geriatric Depression Scale 15 (GDS-15)
  • Fluent in written and spoken Swedish
  • Consents to participate in the trial
Not Eligible

You will not qualify if you...

  • Unable to use patient materials due to visual impairment
  • Unable to communicate with therapist due to hearing impairment
  • Diagnosis of major neurocognitive disorder
  • Score below 25 points on the Mini Mental State Examination (MMSE)
  • Elevated suicide risk
  • Current substance or alcohol use disorder
  • Previous or current psychotic disorder
  • Previous or current bipolar disorder
  • Ongoing psychological treatment or psychotherapy

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - Approximately 2 months

Participants randomized to the intervention receive a five-session brief behavioral activation treatment delivered face-to-face in their home over two months, as an add-on to their usual care. Sessions 1 to 4 occur weekly, and session 5 is a booster session four weeks after session 4.

5 visits (in-person) in participant's home over 2 months, with sessions 1-4 weekly and session 5 four weeks after session 4

Outpatient Treatment

Duration - Ongoing during study period

Participants randomized to usual care continue their care as usual provided by primary care and/or municipal care without additional intervention.

Follow-up

Duration - 12 months post-intervention

All participants complete questionnaires at baseline, 2 months, and at 3, 6, and 12 months post intervention or equivalent timepoints to assess depressive symptoms and other outcomes.

5 questionnaire assessments: baseline, 2 months, 3, 6, and 12 months post intervention or equivalent

Trial Site Locations

Total: 1 location

1

Eskilstuna kommun

Eskilstuna, Sörmland, Sweden

Actively Recruiting

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Research Team

J

Johnny Pellas, PhD

M

Marina Arkkukangas, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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