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Treatment of Depressive Symptoms in Older Individuals in Isolation During Covid-19 (CoviDep)

Primary Purpose

Depression, Depressive Symptoms

Status
Terminated
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Brief Behavioral Activation with Mental Imagery
Minimal Attention Control Intervention
Sponsored by
Uppsala University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring Depression, Depressive Symptoms, Cognitive Behavioral Therapy, Social Isolation, Coronavirus, Pandemic

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Residing in the County of Västmanland
  • Access to telephone
  • Fluent in written and spoken Swedish
  • Reporting clinically significant depressive symptoms above cut-of on depression measures and/or by structured clinical interview

Exclusion Criteria:

  • Severe depression
  • Elevated risk of suicide
  • Current substance use disorder
  • Current or previous manic/hypomanic episodes
  • Current psychotic disorder
  • Current diagnosis of dementia/major neurocognitive disorder
  • Currently receiving psychological therapy

Sites / Locations

  • Adult Psychiatric Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Brief Behavioral Activation with Mental Imagery

Minimal Attention Control Intervention

Arm Description

Four weekly sessions of Brief Behavioral Activation with Mental Imagery.

Four weeks with weekly follow-up calls.

Outcomes

Primary Outcome Measures

Change from baseline in depressive symptoms using the Montgomery-Asberg Depression Rating Scale, MADRS-S
MADRS-S is a nine-item questionnaire used to measure severity of depression. The score ranges from 0-54.

Secondary Outcome Measures

Change from baseline in depressive symptoms using the Geriatric Depression Rating Scale 15, GDS-15
GDS-15 is a 15-item questionnaire used to identify depression in the elderly. The score ranges from 0-15.
Change from baseline in depressive symptoms using the Patient Health Questionnaire 9, PHQ-9
PHQ-9 is a nine-item questionnaire used to identify depression as well as measuring severity of depression. The score ranges from 0-27.
Change in depression diagnosis assessed using the Mini International Neuropsychiatric Interview, MINI
MINI is a structured clinical interview used to assess the presence/absence of common psychiatric disorders.
Change from baseline in anxiety symptoms using the Generalized Anxiety Disorder 7-item, GAD-7
GAD-7 is a seven-item questionnaire used to identify generalized anxiety disorder as well as measuring severity of anxiety symptoms. The score ranges from 0-21.
Change from baseline in behavioral activation using The Behavioral Activation for Depression Scale - Short Form, BADS-SF
BADS-SF is a nine-item questionnaire used to measure changes in avoidance and activation. The score ranges from 0-54.
Change from baseline in health and disability using The WHO Disability Assessment Schedule 12-item, WHODAS
WHODAS-12 is a 12-item questionnaire used to assess disability due to health conditions. The total score ranges from 0-48.
Adverse and unwanted effects of the experimental intervention using the Negative Effects Questionnaire, NEQ
NEQ is a 20-item questionnaire used to assess adverse and unwanted effects of psychological treatments.
Mental imagery is assessed at baseline using the Plymouth Sensory Imagery Questionnaire, Psi-Q
Psi-Q is a 35-item questionnaire assessing the vividness of mental imagery. In this study we plan to use the visual subscale with five items, with a total score ranging from 0-50.

Full Information

First Posted
August 10, 2020
Last Updated
December 29, 2020
Sponsor
Uppsala University
Collaborators
Västmanland County Council, Sweden
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1. Study Identification

Unique Protocol Identification Number
NCT04508868
Brief Title
Treatment of Depressive Symptoms in Older Individuals in Isolation During Covid-19
Acronym
CoviDep
Official Title
Behavioral Activation and Mental Imagery Delivered Via Telephone for the Treatment of Depressive Symptoms in Older Individuals in Isolation During Covid-19: A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Terminated
Why Stopped
Study terminated due to changes in government restrictions. Collected data to be presented as a pilot study.
Study Start Date
August 31, 2020 (Actual)
Primary Completion Date
December 23, 2020 (Actual)
Study Completion Date
December 23, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Uppsala University
Collaborators
Västmanland County Council, Sweden

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This research study is designed to investigate the effects of a brief psychological intervention for improving depressed mood in older individuals (65 years and older) in isolation during the Coronavirus (COVID-19) pandemic. The treatment is delivered by telephone and consists of four weekly individual sessions. Two therapeutic methods are used in combination during this intervention: Behavioral activation (BA) and Mental Imagery (MI). BA involves identifying and scheduling enjoyable and meaningful activities to improve mood and reduce social isolation. To enhance BA efficacy and adherence, MI is paired with BA as MI is known to activate emotion and motivation. The MI intervention in this study involves having participants imagine, in vivid sensory detail, engaging in some of the activities that are scheduled during BA. Approximately 154 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 the intervention after 4 weeks. This procedure makes it possible to evaluate the effects of the treatment while not disadvantaging participants randomized to the control group. Participants will be asked to fill in questionnaires before, during (at the end of each intervention week), and after treatment (or waiting period for the control group). Questionnaires will also be sent 1-, 3- and 6 months after treatment to follow up on the results. A smaller group of participants (10-15) will be asked to participate in a more detailed interview about how they experienced the treatment.
Detailed Description
Coronavirus (COVID-19) has become a worldwide pandemic. The mortality rates are highest in the older age groups, particularly in those 70 years and older. In Sweden, the government urges people 70 years and older to limit close contact with other people and to stay at home as much as possible, a strategy called social distancing. From previous epidemics, such as the SARS-epidemic, we know that quarantine and isolation leads to psychological symptoms such as stress, irritability, depressed mood and sleep problems. About 30% of those subjected to isolation and quarantine become depressed, and in a study from Hong Kong during SARS there was a nearly 32% increase of suicide rates among individuals 65 years and older. In Sweden, depression among the elderly was a major public health concern before the covid-19-pandemic - Major depression occurred in 5-15 % of the older population in Sweden, and one third of the women and a fifth of the men 65 years and older reported subclinical depressive symptoms. Several mental health experts raise concerns that there will be an increase of psychiatric illness during and after covid-19, particularly among the elderly. Depression in older individuals can be treated with antidepressant medication, psychological interventions and physical activity. However, the majority of the older individuals state that they would prefer psychological treatments to medication, which poses a challenge during COVID-19 as such treatments are often delivered face-to-face. Psychological treatments delivered via the Internet are as efficacious as face-to-face, but only 3-4% of the individuals 65 years and above in Sweden use digital applications that replace physical healthcare visits. Psychological treatments have been shown to work when delivered via telephone, and since practically every household in Sweden has access to a telephone, the investigators believe this could be a feasible option. Preferably, the treatment should be brief yet effective, and easily accessible for healthcare professionals. One such treatment is brief behavioral activation (BA), which is aimed at increasing enjoyable and meaningful activities to improve mood. BA has been shown to be feasible in as few as four sessions. Depression is often accompanied by low motivation and lack of energy, which can pose a problem when trying to increase activities. One way of increasing motivation in BA and the likelihood of performing the planned activities is to add mental imagery (MI), where some of these activities are imagined in detail during the calls. However, there are to the investigators knowledge no studies of telephone-delivered brief BA for older individuals, no studies of the combination of BA and MI for depression in the elderly, and no studies of either of these during pandemics with isolation or quarantine. The aim of the present study is to investigate the feasibility, effect and experience of telephone-delivered Behavioral Activation with Mental Imagery for the treatment of depressive symptoms in individuals 65 years and older during the covid-19-pandemic.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Depressive Symptoms
Keywords
Depression, Depressive Symptoms, Cognitive Behavioral Therapy, Social Isolation, Coronavirus, Pandemic

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Brief Behavioral Activation with Mental Imagery
Arm Type
Experimental
Arm Description
Four weekly sessions of Brief Behavioral Activation with Mental Imagery.
Arm Title
Minimal Attention Control Intervention
Arm Type
Placebo Comparator
Arm Description
Four weeks with weekly follow-up calls.
Intervention Type
Behavioral
Intervention Name(s)
Brief Behavioral Activation with Mental Imagery
Intervention Description
Session 1: Provide psychoeducation about depression; Provide treatment rationale for BA; Provide rationale and instructions for activity log; Plan activities for coming week. Session 2: Review activity log; Discuss life goals and values; Plan activities aligned with life goals and values for coming week; Provide rationale for Mental Imagery (MI); Go through MI-exercise for one of the planned activities. Session 3: Review activity log; Troubleshoot any problems carrying out activities; Plan activities aligned with life goals and values for coming week; Go through MI-exercise for one of the planned activities. Session 4: Review activity log; Troubleshoot any problems carrying out activities; Review treatment; Stress the importance of continuing to engage in activities aligned with life goals and values; Referral to additional services if necessary.
Intervention Type
Behavioral
Intervention Name(s)
Minimal Attention Control Intervention
Intervention Description
Weekly call with follow-up of psychiatric symptoms and assessment of suicide risk.
Primary Outcome Measure Information:
Title
Change from baseline in depressive symptoms using the Montgomery-Asberg Depression Rating Scale, MADRS-S
Description
MADRS-S is a nine-item questionnaire used to measure severity of depression. The score ranges from 0-54.
Time Frame
Baseline; Intervention Week 1; Intervention Week 2; Intervention Week 3; Intervention Week 4; 1 month post-intervention; 3 months post-intervention; 6 months post-intervention.
Secondary Outcome Measure Information:
Title
Change from baseline in depressive symptoms using the Geriatric Depression Rating Scale 15, GDS-15
Description
GDS-15 is a 15-item questionnaire used to identify depression in the elderly. The score ranges from 0-15.
Time Frame
Baseline; Intervention Week 4; 1 month post-intervention; 3 months post-intervention; 6 months post-intervention.
Title
Change from baseline in depressive symptoms using the Patient Health Questionnaire 9, PHQ-9
Description
PHQ-9 is a nine-item questionnaire used to identify depression as well as measuring severity of depression. The score ranges from 0-27.
Time Frame
Baseline; Intervention Week 4; 1 month post-intervention; 3 months post-intervention; 6 months post-intervention.
Title
Change in depression diagnosis assessed using the Mini International Neuropsychiatric Interview, MINI
Description
MINI is a structured clinical interview used to assess the presence/absence of common psychiatric disorders.
Time Frame
Baseline; Intervention Week 4.
Title
Change from baseline in anxiety symptoms using the Generalized Anxiety Disorder 7-item, GAD-7
Description
GAD-7 is a seven-item questionnaire used to identify generalized anxiety disorder as well as measuring severity of anxiety symptoms. The score ranges from 0-21.
Time Frame
Baseline; Intervention Week 4; 1 month post-intervention; 3 months post-intervention; 6 months post-intervention.
Title
Change from baseline in behavioral activation using The Behavioral Activation for Depression Scale - Short Form, BADS-SF
Description
BADS-SF is a nine-item questionnaire used to measure changes in avoidance and activation. The score ranges from 0-54.
Time Frame
Baseline; Intervention Week 4; 1 month post-intervention; 3 months post-intervention; 6 months post-intervention.
Title
Change from baseline in health and disability using The WHO Disability Assessment Schedule 12-item, WHODAS
Description
WHODAS-12 is a 12-item questionnaire used to assess disability due to health conditions. The total score ranges from 0-48.
Time Frame
Baseline; Intervention Week 4; 1 month post-intervention; 3 months post-intervention; 6 months post-intervention.
Title
Adverse and unwanted effects of the experimental intervention using the Negative Effects Questionnaire, NEQ
Description
NEQ is a 20-item questionnaire used to assess adverse and unwanted effects of psychological treatments.
Time Frame
Experimental Intervention Week 4.
Title
Mental imagery is assessed at baseline using the Plymouth Sensory Imagery Questionnaire, Psi-Q
Description
Psi-Q is a 35-item questionnaire assessing the vividness of mental imagery. In this study we plan to use the visual subscale with five items, with a total score ranging from 0-50.
Time Frame
Baseline; Intervention Week 4.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Residing in the County of Västmanland Access to telephone Fluent in written and spoken Swedish Reporting clinically significant depressive symptoms above cut-of on depression measures and/or by structured clinical interview Exclusion Criteria: Severe depression Elevated risk of suicide Current substance use disorder Current or previous manic/hypomanic episodes Current psychotic disorder Current diagnosis of dementia/major neurocognitive disorder Currently receiving psychological therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mattias Damberg, MD, PhD
Organizational Affiliation
County of Vastmanland and Uppsala University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Adult Psychiatric Clinic
City
Västerås
State/Province
Västmanland
ZIP/Postal Code
72189
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified outcome measure IPD will be shared upon reasonable requests from academic researchers.
IPD Sharing Time Frame
Study protocol to be shared before data collection is completed Statistical Analysis Plan to be shared before data analysis begin
IPD Sharing Access Criteria
Data will be shared upon reasonable requests assessed by the investigators.

Learn more about this trial

Treatment of Depressive Symptoms in Older Individuals in Isolation During Covid-19

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