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Internet-based Psychotherapy for Depressed Elderly

Not Applicable
Completed
Conditions
Depression
Interventions
Behavioral: Depresijos terapija
Registration Number
NCT04728204
Lead Sponsor
Vilnius University
Brief Summary

This study aims to evaluate the effectiveness of internet-based cognitive behavioral therapy (CBT) for depressed elderly.

Detailed Description

Individuals of age 60+ with symptoms of depression will be assessed before the study. At week 0, participants who meet eligibility requirements will be randomized either to intervention group which will participate in an 8-week internet-based modular CBT or to a delayed treatment control group.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
84
Inclusion Criteria
  • depressive symptoms
  • have access to a computer/tablet/smartphone and to the internet
  • have good knowledge of the Lithuanian language
Exclusion Criteria
  • alcohol addiction
  • presently in any other psychological treatment
  • severe depression
  • suicidal ideation
  • significant change in psychiatric medication (during last 6 weeks)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupDepresijos terapija8 module, 8 week long internet-based intervention for reducing burden of depression
Primary Outcome Measures
NameTimeMethod
Patient Health Questionnaire (PHQ-9)Pre-treatment, week 8, 3, 12 and 24 months post-treatment

Change from baseline in depression symptoms post-treatment (week 8), at three months, at 12 months and at 24 months post-treatment. Measure contains 9 questions that have to be responded to by choosing an answer from a 4-item Likert scale, where number 0 indicates 'Not at all' and 3 - 'Nearly every day'. Higher score indicates more severe symptoms.

Geriatric Depression Scale (GDS)Pre-treatment, week 8, 3, 12 and 24 months post-treatment

Change from baseline in depression symptoms post-treatment (week 8), at three months, at 12 months and at 24 months post-treatment. Measure contains 15 questions that have to be responded 'Yes' or 'No'. Higher score indicates more severe symptoms.

Secondary Outcome Measures
NameTimeMethod
Generalized Anxiety Disorder-7 (GAD-7)Pre-treatment, week 8, 3, 12 and 24 months post-treatment

Change from baseline in anxiety symptoms post-treatment (week 8), at three months, at 12 months and at 24 months post-treatment. Measure contains 7 questions that have to be responded to by choosing an answer from a 4-item Likert scale, where number 0 indicates 'Not at all' and 3 - 'Nearly every day'. Higher score indicates more severe symptoms.

The World Health Organisation- Five Well-Being Index (WHO-5)Pre-treatment, week 8, 3, 12 and 24 months post-treatment

Change from baseline in well-being post-treatment (week 8), at three months, at 12 months and at 24 months post-treatment. WHO-5 contains 5 statements about individuals well-being in the past two weeks. Respondents have to choose the best corresponding answer using a 6-item Likert scale where a score of 0 indicates 'At no time' and a score of 5 - 'All the time'. Higher score indicates higher well-being.

Trial Locations

Locations (1)

Vilnius University

🇱🇹

Vilnius, Lithuania

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