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Treatment of Outpatients With Severe Asthma and Moderate or Severe Major Depressive Disorder

Escitalopram in the Treatment of Outpatients With Severe Asthma and Moderate or Severe Major Depressive Disorder: A Randomized, Double-Blind, Placebo-Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00621946
Enrollment
26
Registered
2008-02-22
Start date
2008-03-31
Completion date
2010-03-31
Last updated
2014-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Moderate or Severe Major Depressive Disorder, Severe Asthma

Keywords

Asthma, Depression, Escitalopram

Brief summary

The purpose is to determine if: 1) Escitalopram treatment will be associated with less oral corticosteroid use than placebo in outpatients with severe asthma and moderate or severe major depressive disorder (MDD). 2) Escitalopram treatment will be associated with greater improvement in asthma symptoms than placebo in outpatients with severe asthma and moderate or severe MDD. 3) Escitalopram treatment will be associated with greater depressive symptom remission rates than placebo in outpatients with severe asthma and moderate or severe MDD.

Detailed description

Primary Aim 1\) Determine if escitalopram treatment is associated with less oral corticosteroid use for asthma symptom control than placebo in asthma outpatients with moderate or MDD. Secondary Aims 1. Determine if escitalopram treatment is associated with greater improvement in asthma symptoms than placebo in outpatients with severe asthma and moderate or severe MDD. 2. Determine if escitalopram treatment is associated with greater depressive symptom remission rates than placebo in outpatients with severe asthma and moderate or severe MDD. Background/Significance Asthma is a common, chronic general medical condition characterized by inflammation and variable, but usually reversible, airflow obstruction. Approximately 7.2% of people in the United States have a history of asthma. Asthma is common with an increasing prevalence and mortality especially in low-income and minority populations. The course of asthma appears to be influenced by mood and emotions. It has been reported that there is a high prevalence of depression or depressive symptoms in both children and adults with asthma. Depression is associated with increased use of asthma-related urgent care services, as well as a variety of unfavorable asthma outcomes. In addition to the possible associations between depression and asthma medication nonadherence and even death, depression appears to be associated with increased use of emergency rooms, hospitals, and unscheduled appointments for asthma. Despite data on the frequency of depression in asthma and its adverse consequences, it is generally not recognized or treated. Our proposed study is different. We observed a modest difference between antidepressant and placebo in a prior trial. However, in a subgroup with more severe asthma (based on frequent corticosteroid use) and more severe depression (based on higher depressive symptoms scores) we saw a much larger effect size. The proposed study will target this subgroup. The sample size is based on the effect size we observed in this subgroup in our previous pilot study. A placebo controlled trial is needed because 1) the primary outcome in our previous trial was not significant. Therefore, it is not clear that antidepressant treatment is effective in depressed asthma patients. 2) We identified a subgroup with greater depressive symptom and asthma severity that based on a post-hoc analysis appeared to show a favorable response to the antidepressant. Thus, we want to confirm these post-hoc findings with a targeted prospective study. In the clinical population we will study, very few patients have ever received assessment or treatment for depression. Therefore, we would not be withholding clearly effective treatment that they would otherwise receive. Standard of care for severe asthma is aggressive asthma treatment. Our study does not require any changes in the patient's asthma treatment. No guidelines are currently available on the treatment of depression in asthma patients. Standard care for depression would be antidepressants.

Interventions

DRUGPlacebo

Placebo Matching Escitalopram

DRUGEscitalopram

Active Escitalopram

Sponsors

Forest Laboratories
CollaboratorINDUSTRY
University of Texas Southwestern Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Current HAM-D score of ≥ 20 * Patients with severe asthma (defined as asthma requiring three or more course of oral corticosteroids in the past year). * No changes in asthma medications, oral corticosteroid use, or treatment for respiratory tract infections in the past week * Needs to have taken ≥ 3 courses of oral corticosteroids, for asthma, in the past 12 months. * Both male and female * English- or Spanish-speaking

Exclusion criteria

* Current substance or alcohol abuse/dependence * MDD with psychotic features (delusions, hallucinations, disorganized thought processes) * Bipolar disorder * Schizophrenia or schizoaffective disorder * Substance-induced mood disorder and mood disorder secondary to a general medical condition * Mental retardation or other severe cognitive impairment * Prison or jail inmates * Pregnant or nursing women or women of childbearing age who will not use The University of Texas Southwestern Medical Center - Institutional Review Board (UTSW IRB) approved methods of birth control or abstinence during the study * Treatment-resistant depressed persons defined as having failed two adequate trials of antidepressants * Current antipsychotic or antidepressant therapy or psychotherapy * Initiation of other psychotropic medications or psychotherapy within past 2 weeks (e.g., anxiolytics, hypnotics)

Design outcomes

Primary

MeasureTime frameDescription
HAM-D (Hamilton Rating Scale for Depression)BaselineThe HAM-D is a 17 item questionnaire (a clinician-administered depression scale) designed to evaluate severity of depressive symptoms. Scores can range from 0 to 52. The higher the score, the worse the depressive symptoms (worse outcome).
ACQ (Asthma Control Questionnaire)BaselineThe ACQ is a questionnaire used to assess symptoms pertinent to asthma management. Scores range from 0 to 42. The higher the score, the worse the asthma symptoms (worse outcome). The total ACQ score is obtained by dividing the raw score by the total number of items (in this case 7 items).
IDS-SR (Inventory of Depressive Symptomatology - Self-Report)BaselineThe IDS-SR is a 30 item (self-report questionnaire) designed to assess symptoms of depression. Scores range from 0 to 90. The higher the score, the worse the depressive symptoms (worse outcome).

Countries

United States

Participant flow

Participants by arm

ArmCount
Escitalopram
Active Escitalopram (A SSRI) taken orally in 10mg or 20mg doses daily.
13
Placebo
Placebo Matching Escitalopram taken orally daily.
12
Total25

Baseline characteristics

CharacteristicEscitalopramTotalPlacebo
Age, Continuous42.5 years
STANDARD_DEVIATION 9.8
45.4 years
STANDARD_DEVIATION 11.5
48.6 years
STANDARD_DEVIATION 12.7
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
6 Participants10 Participants4 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
3 Participants5 Participants2 Participants
Race (NIH/OMB)
White
4 Participants10 Participants6 Participants
Region of Enrollment
United States
13 participants25 participants12 participants
Sex: Female, Male
Female
8 Participants14 Participants6 Participants
Sex: Female, Male
Male
5 Participants11 Participants6 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 130 / 12
serious
Total, serious adverse events
2 / 131 / 12

Outcome results

Primary

ACQ (Asthma Control Questionnaire)

The ACQ is a questionnaire used to assess symptoms pertinent to asthma management. Scores range from 0 to 42. The higher the score, the worse the asthma symptoms (worse outcome). The total ACQ score is obtained by dividing the raw score by the total number of items (in this case 7 items).

Time frame: Baseline

ArmMeasureValue (MEAN)Dispersion
EscitalopramACQ (Asthma Control Questionnaire)1.9 units on a scaleStandard Deviation 1.1
PlaceboACQ (Asthma Control Questionnaire)2.9 units on a scaleStandard Deviation 0.9
Primary

ACQ (Asthma Control Questionnaire)

The ACQ is a questionnaire used to assess symptoms pertinent to asthma management.Scores range from 0 to 42. The higher the score, the worse the asthma symptoms (worse outcome). The total ACQ score is obtained by dividing the raw score by the total number of items (in this case 7 items).

Time frame: Up to 12 weeks

ArmMeasureValue (MEAN)Dispersion
EscitalopramACQ (Asthma Control Questionnaire)1.9 units on a scaleStandard Deviation 1.4
PlaceboACQ (Asthma Control Questionnaire)2.4 units on a scaleStandard Deviation 1.2
Primary

HAM-D (Hamilton Rating Scale for Depression)

The HAM-D is a 17 item questionnaire (a clinician-administered depression scale) designed to evaluate severity of depressive symptoms. Scores can range from 0 to 52. The higher the score, the worse the depressive symptoms (worse outcome).

Time frame: Baseline

ArmMeasureValue (MEAN)Dispersion
EscitalopramHAM-D (Hamilton Rating Scale for Depression)24.8 units on a scaleStandard Deviation 4.4
PlaceboHAM-D (Hamilton Rating Scale for Depression)28.3 units on a scaleStandard Deviation 5.1
Primary

HAM-D (Hamilton Rating Scale for Depression)

The HAM-D is a 17 item questionnaire (a clinician-administered depression scale) designed to evaluate severity of depressive symptoms. Scores can range from 0 to 52. The higher the score, the worse the depressive symptoms (worse outcome).

Time frame: Up to 12 weeks

ArmMeasureValue (MEAN)Dispersion
EscitalopramHAM-D (Hamilton Rating Scale for Depression)16.7 units on a scaleStandard Deviation 11.4
PlaceboHAM-D (Hamilton Rating Scale for Depression)17.7 units on a scaleStandard Deviation 7.6
Primary

IDS-SR (Inventory of Depressive Symptomatology - Self-Report)

The IDS-SR is a 30 item (self-report questionnaire) designed to assess symptoms of depression. Scores range from 0 to 90. The higher the score, the worse the depressive symptoms (worse outcome).

Time frame: Baseline

ArmMeasureValue (MEAN)Dispersion
EscitalopramIDS-SR (Inventory of Depressive Symptomatology - Self-Report)35.2 units on a scaleStandard Deviation 15
PlaceboIDS-SR (Inventory of Depressive Symptomatology - Self-Report)42.9 units on a scaleStandard Deviation 12.3
Primary

IDS-SR (Inventory of Depressive Symptomatology - Self-Report)

The IDS-SR is a 30 item (self-report questionnaire) designed to assess symptoms of depression. Scores range from 0 to 90. The higher the score, the worse the depressive symptoms (worse outcome).

Time frame: Up to 12 weeks

ArmMeasureValue (MEAN)Dispersion
EscitalopramIDS-SR (Inventory of Depressive Symptomatology - Self-Report)26.3 units on a scaleStandard Deviation 17.4
PlaceboIDS-SR (Inventory of Depressive Symptomatology - Self-Report)24.6 units on a scaleStandard Deviation 14.9

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026