Behavioral Activation for Depression: A Randomized Controlled Trial
Primary Purpose
Depression
Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Behavioral activation
Sponsored by
About this trial
This is an interventional treatment trial for Depression
Eligibility Criteria
Depressed participants:
Inclusion Criteria:
- A principal diagnosis of major depressive disorder (MDD) according to DSM-5 of a mild to moderate severity, that is, a 4 on a 0 (no depressive symptoms) to 8 (very severe symptoms) scale according to the ADIS-5 interview.
- Danish language proficiency.
- Ability and willingness to give informed consent.
- Be either non-medicated or stabilized [i.e., same dosage for a minimum of 8 weeks on antidepressant and antianxiety medication].
- Access to either a smartphone, tablet, or computer with video camera
Exclusion Criteria:
- Severe depression deemed to require more intense psychotherapy or medication.
- Non-stabilized medication (see above).
- A history of bipolar disorder.
- Current or past psychosis.
- Substance abuse or dependence judged to require treatment.
- Suicide risk requiring immediate hospitalization.
- Receiving any other current psychotherapy or counseling.
Healthy participants:
Will only be considered for participation if they can read and understand the Danish language and deemed able and willing to give informed consent. They will undergo diagnostic interviewing to ensure the absence of a current psychiatric diagnosis and the absence of a history of bipolar disorder or psyhosis according to the ADIS-5. They will also be excluded if they receive any psychotropic medication.
Sites / Locations
- Aarhus University - Institute of Psychology and Behavioral SciencesRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
No Intervention
Arm Label
mBA
BA
Waitlist
Arm Description
Motor enhanced behavioral activation. 10 sessions.
Standard behavioral activation. 10 sessions.
10 week waitlist.
Outcomes
Primary Outcome Measures
Depressive symptoms (PHQ-9)
Patient Health Questionnaire-9 (Spitzer et al., 1999; Spitzer et al., 2000)
Secondary Outcome Measures
Depressive symptoms (PHQ-9)
Patient Health Questionnaire-9 (Spitzer et al., 1999; Spitzer et al., 2000)
Number of recovered patients in BA/mBA vs. waitlist
Number cacluated according to the minimal clinically important difference for the PHQ-9 (i.e., 5 score points; Lowe, Unutzer, Callahan, Perkins, & Kroenke, 2004)
Number of patients having obtained a reliable change in depressive symptoms in BA/mBA vs. waitlist
Calculated according to the reliable change index (Jacobsen & Truax, 1999) for the PHQ-9.
Exposure to environmental rewards (EROS)
The Environmental Reward Observation Scale (Armento & Hopko, 2007)
Intereoceptive awareness (MAIA)
The Multidimensional Assessment of Interoceptive Awareness, Version 2 (Mehling, Acree, Stewart, Silas, & Jones, 2018)
Behavioral activation and inhibition (BIS/BAS)
BIAS/BAS (Carver & White, 1994)
Perceived coping ability(CSES)
The Coping Self-Efficacy Scale (Chesney, Neilands, Chambers, Taylor, & Folkman, 2006
Rumination (RRS)
The Ruminative Response Scale, brooding subscale (Treynor, Gonzalez, & Nolen-Hoeksema, 2003)
Worry (PSWQ)
The Penn State Worry Questionnaire (Meyer, Miller, Metzger, & Borkovec, 1990)
Decentering (EQ)
The Experiences Questionnaire Decentering subscale (Fresco et al., 2007)
Dysfunctional attitudes (DAS)
Dysfuntional Attitude Scale SF1 (Beever et al., 2009; Weismann, 1979)
Quality of life (QoL)
The World Health Organization (WHO)-5 questionnaire
Full Information
NCT ID
NCT04700774
First Posted
December 21, 2020
Last Updated
November 2, 2022
Sponsor
University of Aarhus
1. Study Identification
Unique Protocol Identification Number
NCT04700774
Brief Title
Behavioral Activation for Depression: A Randomized Controlled Trial
Official Title
Behavioral Activation for Depression: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 20, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Aarhus
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The present study is a randomized controlled trial that will evaluate two versions of behavioral activation (BA); one version which is a standard BA program and one which is a motor enhanced BA program (mBA). In both programs, the patient will receive all standard BA interventions, whereas these - in the mBA program - will be supplemented with interventions focused on noticing and manipulating posture and movement associated with action initiation. The mBA program builds upon recent evidence pointing to motor manipulations of posture and movement as having the potential to assist in action initiation and thus following through with the planned activity schedule. Previous research has shown that patient compliance with the activity schedule is causally associated with depression reduction, which will be explored as a mediator of treatment gains.
Detailed Description
Depression is a leading cause of disability worldwide (WHO, 2020). Nationally, more than 10.000 new cases of depression are registered each year with a higher frequency in women (Sundhedsstyrelsen, 2015). With depression comes reduced quality of life for the affected individual and a great economic burden for society. For instance, collectively, people with depression have more than 600.000 more visits to their general practitioner (GP) than people without depression, and when employed, they have 1.7 million more sick days than people without depression (Sundhedsstyrelsen, 2015). Access to effective treatment is thus crucial. Behavioral activation (BA) is an efficacious psychological treatment for depression; its effect may exceed that of medication and is equal to that of cognitive behavioral therapy (CBT) (Cuijpers, van Straten, & Warmerdam, 2007; Ekers et al., 2014). BA is therefore recommended as a first-line psychological treatment for mild to moderate depression by the National Institute for Health and Care Excellence (NICE CG90; 2009).
Depression is often described with reference to the disorder's cognitive characteristics, such as the depressogenic content of thoughts ( Beck, Rush, Shaw, & Emery, 1979) and the tendency to engage rumination and self-criticism (e.g., Mennin & Fresco, 2013) as well as behavioral characteristics such as lack of motivation, avoidance, and withdrawal (e.g., Lewinsohn, 1974). Although less commonly found in the description of depression, research has also documented bodily characteristics, including alterations to the motor system. Concerning the motor system, gait patterns associated with sadness and depression have been characterized by reduced walking speed, arm swing, and vertical head movements (Michalak et al., 2009). Successful treatment of depression thus may include - not only improvements in cognition and behavior - but also normalization of the motor system.
Although CBT and BA produce similar results in the treatment of depression, they are rooted in different theoretical models of depression. Traditional CBTs target the depressed individual's dysfunctional appraisals. They do so by inviting the client to restructure their thinking and expose themselves to situations that will help them in this endeavor. This is based on the assumption that the root of the problematic behavior in depression, first and foremost, is a result of dysfunctional thinking (e.g., "it doesn't matter anyway", "I will always be depressed") ( Beck et al., 1979). BA, on the other hand, is primarily rooted in a behavioral theory of depression. It builds on Lewinsohn's (1974) seminal work, holding that depression is the result of a loss or lack of response-contingent positive reinforcement, leaving the patient stuck in a maladaptive pattern of behavioral avoidance and withdrawal, preventing them from having rewarding interactions with their surroundings. In order to combat this avoidance and withdrawal behavior permeating depression, the patient in BA is invited to monitor their activities - mapping the dysfunctional patterns - and then to engage in activities that are important and joyful, if not at first, then over time (Lejuez, Hopko, Acierno, Daughters, & Pagoto, 2011; Martell, Dimidjian, & Herman-Dunn, 2010). Indeed, in the beginning, certain activities may not feel instantly rewarding, and the depressed person may only have a vague memory of a time when that activity was associated with joy. However, in BA, patients are invited to try to act 'outside-in', instead of 'inside-out', meaning that they refrain from acting according to their mood (low mood will likely lead to more avoidance and withdrawal behavior) and instead approach the planned activity regardless of their current mood (i.e., outside-in).
Previous research has shown that patient compliance with the activity schedule is causally associated with depression reduction (Ryba et al., 2014). Thus, theoretically and empirically, following through with the activity schedule presents as one of the most important mediators of treatment gains. However, patients may struggle with initiating the planned activities. In a sense, BA asks patients to do exactly the thing they feel like they cannot do, that is, get up and get going. Despite psychoeducation about the rationale of the treatment, and even when clients get initial experience with the fact that they feel better and more competent after a certain activity, they may still struggle with action initiation (Martell et al., 2010). Recent evidence points to motor manipulations of posture and movement as having the potential to be an important supplementary intervention within BA, enhancing the likelihood that clients follow through with the planned activity schedule. In a recent meta-analysis, we investigated the effect of motor manipulations (i.e., expansive/upright and contractive/slumped postures) on affective and behavioral outcomes. Across studies, we found that the manipulation of motor activity altered mood, emotions, and actions such that when individuals adopt neutral or expansive postures, they reported better mood, more positive emotions, and engaged in more approach behavior than when assuming contractive postures (Elkjær et al., 2020). These results could suggest that adopting neutral or expansive postures could be helpful for depressed individuals in initiating action.
Building on the solid findings from previous BA trials and the recent findings concerning the effects of motor manipulations, the present study is a randomized controlled trial that will evaluate two versions of BA, one version which is a standard BA program (Lejuez et al., 2011) and one which is a motor enhanced BA program (mBA). In both programs, the patient will receive all standard BA interventions, whereas these - in the mBA program - will be supplemented with interventions focused on noticing and manipulating posture and movement associated with action initiation. One hundred and seventeen individuals diagnosed with major depressive disorder (MDD) will be randomized to active treatment or a 10-week waitlist followed by active treatment. The active treatment is also based upon randomization, where individuals will receive either standard BA or mBA, and will be followed for 6 months post treatment. In the active treatment, individuals will receive 10 weekly video sessions, conducted using the secure and GDPR-approved video-conference program 'Zoom'.
Before and after the mBA program, patients will partake in an experiment. The effect of motor manipulations on responses to two different personally relevant emotional conflicts will be evaluated. One emotional conflicts will be one that is typical of those detected in depression, where an individual wishes they could or would enjoy approaching a situation but lack the motivation to do so (i.e., approach vs. withdrawal). The other will be one in which an individual wishes they could approach a situation but feel scared or nervous about doing so (approach vs. avoidance). Participants will be randomized to one of three experimental conditions: adopting expansive postures, contractive postures, or neutral postures. Effects will be evaluated concerning action tendencies, behavioral self-efficacy and experienced emotions. For the experiment taking place before treatment, patients will be compared to a group of matched healthy controls.
Hypotheses
It is hypothesized that 1) both BA and mBA will be more efficacious in reducing symptoms of depression than the waitlist, and 2) gains are expected to be maintained through the follow-up period.
It is also expected that 3) mBA with its extra treatment component focused on the motor system will be superior to BA of at least small magnitude (d=0.3; Bell et al., 2013). This added benefit of mBA is expected to be driven by compliance with the activity schedule as it is hypothesized 4) that the mBA condition can increase success with planned activities (i.e., quantity of completed activities and proportion of completed activities). 5) This success with planned activities is expected to mediate treatment gains in both BA and mBA.
Concerning the experiment, before treatment, 6) it is expected that depressed patients to show less approach behavior (i.e., less approach action tendencies, less behavioral self-efficacy, , and less positive emotions) in response to the emotional conflicts compared with healthy controls. Furthermore, 7) it is hypothesized that participants assuming neutral and expansive postures will respond with more approach behavior than participants adopting contractive postures. 8) Effects will be explored between groups (healthy vs clinical), thereby determining if the neutral and expansive motor displays are more or less facilitative of approach behavior, and if the contractive motor displays are more or less detrimental to such behavior, depending on clinical status. 9) Effects will also be explored comparing the two types of emotional conflicts.
Concerning the experiment following treatment, 10) it is expected that any differences between the healthy and clinical group detected at baseline will diminish or disappear, reflecting clinical improvement and normalization following treatment.
Collaborators:
Mai B. Mikkelsen, Gitte Tramm, Emme Elkjær, Kaj Sparle Christensen, Douglas S. Mennin, & Johannes Michalak
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Participants will be randomized to active treatment or a 10-week waitlist followed by active treatment (BA or mBA). The active treatment is also based upon randomization, where individuals will receive either standard BA or mBA, and will be followed for 6 months post treatment.
Masking
Participant
Masking Description
It will not be known to participants whether they receive standard BA or mBA.
Allocation
Randomized
Enrollment
117 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
mBA
Arm Type
Experimental
Arm Description
Motor enhanced behavioral activation. 10 sessions.
Arm Title
BA
Arm Type
Experimental
Arm Description
Standard behavioral activation. 10 sessions.
Arm Title
Waitlist
Arm Type
No Intervention
Arm Description
10 week waitlist.
Intervention Type
Behavioral
Intervention Name(s)
Behavioral activation
Intervention Description
Brief Behavioral Activation Treatment with and without motor enhancement. All patients will receive 10 online video sessions. BA focuses on increasing overt behaviors to bring patients into contact with reinforcing environmental contingencies and corresponding improvements in thoughts, mood, and quality of life (Hopko, Lejuez, et al., 2003). BA follows the basic behavioral principles of extinction, shaping, fading, and in vivo exposure (Hopko & Lejuez, 2007; Lejuez et al., 2001, 2011). In the mBA condition only a) patients will be introduced to the idea that the motor system can be used in the service of action initiation and will receive an audio recording with motor manipulations to assist in action initiation and b) the therapist will conduct imaginary behavioral activation and - in session - complete questionnaires identical to those in the experiment before and after the bodily instructions presented in the treatment.
Primary Outcome Measure Information:
Title
Depressive symptoms (PHQ-9)
Description
Patient Health Questionnaire-9 (Spitzer et al., 1999; Spitzer et al., 2000)
Time Frame
Change from pre to post (10 weeks) active treatment.
Secondary Outcome Measure Information:
Title
Depressive symptoms (PHQ-9)
Description
Patient Health Questionnaire-9 (Spitzer et al., 1999; Spitzer et al., 2000)
Time Frame
Change from pre-treatment through 6-months follow-up
Title
Number of recovered patients in BA/mBA vs. waitlist
Description
Number cacluated according to the minimal clinically important difference for the PHQ-9 (i.e., 5 score points; Lowe, Unutzer, Callahan, Perkins, & Kroenke, 2004)
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Number of patients having obtained a reliable change in depressive symptoms in BA/mBA vs. waitlist
Description
Calculated according to the reliable change index (Jacobsen & Truax, 1999) for the PHQ-9.
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Exposure to environmental rewards (EROS)
Description
The Environmental Reward Observation Scale (Armento & Hopko, 2007)
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Intereoceptive awareness (MAIA)
Description
The Multidimensional Assessment of Interoceptive Awareness, Version 2 (Mehling, Acree, Stewart, Silas, & Jones, 2018)
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Behavioral activation and inhibition (BIS/BAS)
Description
BIAS/BAS (Carver & White, 1994)
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Perceived coping ability(CSES)
Description
The Coping Self-Efficacy Scale (Chesney, Neilands, Chambers, Taylor, & Folkman, 2006
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Rumination (RRS)
Description
The Ruminative Response Scale, brooding subscale (Treynor, Gonzalez, & Nolen-Hoeksema, 2003)
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Worry (PSWQ)
Description
The Penn State Worry Questionnaire (Meyer, Miller, Metzger, & Borkovec, 1990)
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Decentering (EQ)
Description
The Experiences Questionnaire Decentering subscale (Fresco et al., 2007)
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Dysfunctional attitudes (DAS)
Description
Dysfuntional Attitude Scale SF1 (Beever et al., 2009; Weismann, 1979)
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Title
Quality of life (QoL)
Description
The World Health Organization (WHO)-5 questionnaire
Time Frame
Change form pre to post active treatment (10 weeks) and change from pre-treatment through 6-months follow-up
Other Pre-specified Outcome Measures:
Title
PHQ-9
Description
Depressive symptoms will be evaluted session by session for mediation analyses
Time Frame
Session by session change during the 10 weeks of active treatment
Title
EROS
Description
Environmental rewards will be evaluted session by session for mediation analyses
Time Frame
Session by session change during the 10 weeks of active treatment
Title
CSES
Description
Coping ability will be evaluted session by session for mediation analyses
Time Frame
Session by session change during the 10 weeks of active treatment
Title
RRS
Description
Ruminaiton will be evaluted session by session for mediation analyses
Time Frame
Session by session change during the 10 weeks of active treatment
Title
Activity log (kept by therapist)
Description
Quantity and proportion of activities will be calculated for mediation analyses
Time Frame
Session by session change during the 10 weeks of active treatment
Title
EQ
Description
Decentering ability will be tested as a competing mediator
Time Frame
Session by session change during the 10 weeks of active treatment
Title
DAS
Description
Dysfunctional attitudes will be tested as a competing mediator
Time Frame
Session by session change during the 10 weeks of active treatment
Title
Overall activity level
Description
Total steps taken (measured by pedometer) and exercise each day will be tested as a competing mediator
Time Frame
Session by session change during the 10 weeks of active treatment
Title
Perceived importance of activity
Description
"How important is the activity to you?". Outcome in experiment (7-point Likert scale from 1 to 7)
Time Frame
Change from pre to post experimental manipulation (10 minutes) (pre-treatment only for healthy participants, pre- and post-treatment for depressed participants)
Title
Expected effect of activity on mood
Description
"How do you expect the activity to affect your mood?" Outcome in experiment (7-point Likert scale from -3 [negative] to +3 [positive])
Time Frame
Change from pre to post experimental manipulation (10 minutes) (pre-treatment only for healthy participants, pre- and post-treatment for depressed participants)
Title
Perceived self-efficacy concerning activity
Description
"How confident do you feel about your ability yo take the activity?". Outcome in experiment (7-point Likert scale from 1 to 7)
Time Frame
Change from pre to post experimental manipulation (10 minutes) (pre-treatment only for healthy participants, pre- and post-treatment for depressed participants)
Title
Perceived difficulty of completing activity
Description
"How difficult is it for you to do the activity". Outcome in experiment (7-point Likert scale from 1 to 7)
Time Frame
Change from pre to post experimental manipulation (10 minutes) (pre-treatment only for healthy participants, pre- and post-treatment for depressed participants)
Title
Degree of avoidance and withdrawal motivation concerning activity
Description
Withdrawal: "I do no feel like or have the energy to complete the activity." Avoidance: "I am scared, nervous or worried about doing the activity". Outcome in experiment (7-point Likert scale from 1 to 7)
Time Frame
Change from pre to post experimental manipulation (10 minutes) (pre-treatment only for healthy participants, pre- and post-treatment for depressed participants)
Title
Action tendencies (DAT; O'Toole & Mikkelsen, 2020) concerning activity
Description
Outcome in experiment (8 drawings rated on a 5-point Likert scale from 1 to 5)
Time Frame
Change from pre to post experimental manipulation (10 minutes) (pre-treatment only for healthy participants, pre- and post-treatment for depressed participants)
Title
Negative and positive emotions when thinking about doing activity
Description
8 negative and 7 positive emotions used as outcome in experiment (5-point Likert scale from 1 to 5)
Time Frame
Change from pre to post experimental manipulation (10 minutes) (pre-treatment only for healthy participants, pre- and post-treatment for depressed participants)
Title
State rumination (Brief State Rumination Inventory [BRSI]; Marchetti, Mor, Chiorri, & Koster, 2018)
Description
Outcome in experiment (statements rated from 0 to 100)
Time Frame
Obtained post experiment only
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Depressed participants:
Inclusion Criteria:
A principal diagnosis of major depressive disorder (MDD) according to DSM-5 of a mild to moderate severity, that is, a 4 on a 0 (no depressive symptoms) to 8 (very severe symptoms) scale according to the ADIS-5 interview.
Danish language proficiency.
Ability and willingness to give informed consent.
Be either non-medicated or stabilized [i.e., same dosage for a minimum of 8 weeks on antidepressant and antianxiety medication].
Access to either a smartphone, tablet, or computer with video camera
Exclusion Criteria:
Severe depression deemed to require more intense psychotherapy or medication.
Non-stabilized medication (see above).
A history of bipolar disorder.
Current or past psychosis.
Substance abuse or dependence judged to require treatment.
Suicide risk requiring immediate hospitalization.
Receiving any other current psychotherapy or counseling.
Healthy participants:
Will only be considered for participation if they can read and understand the Danish language and deemed able and willing to give informed consent. They will undergo diagnostic interviewing to ensure the absence of a current psychiatric diagnosis and the absence of a history of bipolar disorder or psyhosis according to the ADIS-5. They will also be excluded if they receive any psychotropic medication.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mia S O'Toole, PhD
Phone
+4587165289
Email
mia@psy.au.dk
Facility Information:
Facility Name
Aarhus University - Institute of Psychology and Behavioral Sciences
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mia S O'Toole, PhD
Phone
+4587165289
Email
mia@psy.au.dk
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Behavioral Activation for Depression: A Randomized Controlled Trial
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