Behavioral Activation-Rehabilitation to Improve Depressive Symptoms & Physical Function After Acute Respiratory Failure (BEHAB)
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|ClinicalTrials.gov Identifier: NCT03431493|
Recruitment Status : Recruiting
First Posted : February 13, 2018
Last Update Posted : May 11, 2022
|Condition or disease||Intervention/treatment||Phase|
|Respiratory Insufficiency Depression Rehabilitation Critical Care||Behavioral: Behavioral Activation - Rehabilitation||Not Applicable|
A growing number of Acute Respiratory Failure (ARF) survivors are burdened by depressive symptoms and physical impairments that last for years after intensive care unit discharge. Notably, depressive symptoms are independently associated with subsequent development of new impairments in physical functioning. There is a lack of treatment options to address these impairments in ARF survivors, with past research suggesting combining treatment for mental and physical health might be more successful.
Therefore, this study is designed to evaluate:
- The feasibility (primary outcome) of participant recruitment and retention in a pilot randomized controlled trial (RCT) of an intervention combining Behavioral Activation (an evidence-based psychological treatment for depression) and physical rehabilitation delivered via telephone and 2 home visits over 12-weeks versus a "usual care" control group.
- The efficacy (secondary outcome) of this Behavioral Activation-Rehabilitation intervention to reduce depressive symptoms and improve physical functioning.
- Modifiable psychosocial risk factors for depressive symptoms in ARF survivors and the association between the intervention and these modifiable factors.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||54 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Official Title:||A Pilot, Feasibility Randomized Controlled Trial of a Behavioral Activation And Rehabilitation Intervention To Improve Psychological And Physical Impairments In Acute Respiratory Failure Survivors|
|Actual Study Start Date :||March 2, 2018|
|Estimated Primary Completion Date :||June 2022|
|Estimated Study Completion Date :||June 2023|
Experimental: Behavioral Activation - Rehabilitation
Behavioral Activation - Rehabilitation
Behavioral: Behavioral Activation - Rehabilitation
Participants will first receive a home visit from a physical therapist (PT) who will evaluate home safety and establish/verify the participant's exercise prescription. Within 1 week, an occupational therapist (OT) will visit the home to: 1) explain the purpose of behavioral activation (BA); 2) help the participant identify long-term recovery goals regarding "valued activities"; and 3) then, using the principles of BA, identify short-term goals for the next week and an action plan. The OT will then call the participant weekly (weeks 2-5) to review the status of the prior week's goals and use BA to set new goals for the upcoming week. The PT and OT will repeat home visits at week 6 to assess the participant's progress, and the OT will conduct phone calls every 2 weeks for weeks 8-12.
No Intervention: Usual Care Control
Usual Care Control
- Feasibility measure per participant [ Time Frame: End of intervention (12 weeks) ]Total number of intervention phone calls completed per patient as a proportion of the number of intervention phone calls each patient is intended to complete.
- Total feasibility measure [ Time Frame: End of intervention (12 weeks) ]Total number of intervention phone calls completed by all study participants as a proportion of total intervention phone calls expected in the study
- Feasibility measure/Assess loss to follow-up [ Time Frame: End of intervention (12 weeks) ]Number of patients completing all study follow-up sessions as a proportion of the number of patients enrolled.
- Feasibility measure [ Time Frame: End of intervention (12 weeks) ]Number of patients enrolled per month
- Hospital Anxiety and Depression Scale (HADS) [ Time Frame: End of intervention (12 weeks) ]An instrument used to assess depressive and anxiety symptoms. Scores for each subscale range from 0 to 21. A HADS score ≥8 indicates clinically important symptoms on either subscale.
- Personal Health Questionnaire - 8 item version (PHQ-8) [ Time Frame: End of intervention (12 weeks) ]The PHQ-8 uses a 4-point Likert scale to assess depressive symptoms. The score range is 0 to 27. Scores 5-9 indicate "mild" symptoms, 10-14 "moderate", and ≥20 "severe" depressive symptoms.
- Diagnostic and Statistical Manual of Mental Disorders (DSM-5) (SCID-5) [ Time Frame: End of intervention (12 weeks) ]A clinical interview to assess depressive symptoms. This is a qualitative assessment.
- Activity Measure for Post-Acute Care Computer Adaptive Test (AMPAC-CAT) [ Time Frame: Baseline, end of intervention (12 weeks) ]The AMPAC-CAT, a measure of physical function, has 269 items across three domains (basic mobility, daily activity and applied cognitive). The computer adaptive test requires a mean of 22 items from the item bank. Scores are norm-based.
- EQ-5D-5L [ Time Frame: End of intervention (12 weeks) ]The EQ-5D-5L is an instrument developed by the EuroQol group to measure health status. The Eq-5D-5L has 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels, ranging from 1 (no problems) to 5 (extreme problems). The resulting health utility score ranges from -0.11 to 1.00. The EQ-5D-5L also records the respondent's self-rated health on a visual analog scale (0 to 100).
- Healthcare Utilization [ Time Frame: End of intervention (12 weeks) ]Patient interview to assess the following post-discharge variables: inpatient readmissions (hospitals, skilled nursing facilities, acute and sub-acute rehabilitation facilities) and outpatient mental health and physical rehabilitation services
- Brief Coping with Problems Experienced (Brief COPE) [ Time Frame: Baseline, end of intervention (12 weeks) ]A 28-item measure of coping strategies with responses provided using a 4-point Likert scale. Scores are provided for the 14 subscales, each of which corresponds to a specific coping strategy (minimum score=2 to maximum score=8).
- Behavioral Activation for Depression SCALE (BAS) [ Time Frame: Baseline, end of intervention (12 weeks) ]This is a 25-item scale that measures changes in avoidance and activation over the course of Behavioral Activation treatment using a 7 point scale (0=not at all to 6=completely). The scale is grouped into 4 subscales (Activation, Avoidance/Rumination, Work/School Impairment, and Social Impairment). To calculate a total score, items on all subscales other than Activation are reverse-coded and then an unweighted sum is computed.
- Connor-Davidson Resilience Scale (CD RISC) [ Time Frame: Baseline, end of intervention (12 weeks) ]This is a 25-item scale with each item rated on a 5-point scale (higher scores indicating greater resilience). The total score ranges from 0 to 100.
- Number of phone attempts needed by the OT to reach the participant for each session [ Time Frame: End of intervention (12 weeks) ]Measure of adherence
- Proportion of sessions fully completed and partially completed [ Time Frame: End of intervention (12 weeks) ]Measure of adherence
- Montreal Cognitive Assessment (MoCA) - BLIND [ Time Frame: End of intervention (12 weeks) ]Measure of cognitive impairment
- Impact of Events Scale - Revised (IES-R) [ Time Frame: End of intervention (12 weeks) ]This is a measure the subjective response to a specific traumatic event (in this case - critical illness and associated ICU experience). The IES-R consists of 22 items, each rated on a 5-point scale; item scores are averaged to generate a mean total score (range: 0-4).
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03431493
|Contact: Albahi M Malikfirstname.lastname@example.org|
|United States, Maryland|
|Johns Hopkins University||Recruiting|
|Baltimore, Maryland, United States, 21205|
|Principal Investigator:||Ann M Parker, MD||Johns Hopkins University|