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Problem-Solving Therapy for People With Major Depression and Chronic Obstructive Pulmonary Disease

Treating Older Patients With Major Depression and Severe COPD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00601055
Enrollment
101
Registered
2008-01-25
Start date
2008-02-29
Completion date
2015-08-31
Last updated
2016-07-15

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

Conditions

Depression, Pulmonary Disease, Chronic Obstructive

Keywords

COPD, Geriatric Depression, Problem-Solving Therapy, Treatment Adherence

Brief summary

This study will evaluate the effectiveness of problem-solving therapy combined with treatment adherence procedures in treating older people with major depression and chronic obstructive pulmonary disease.

Detailed description

Depression is a serious illness that affects a person's mood, thoughts, and physical well-being. Common symptoms of depression include persistent feelings of anxiety, guilt, or hopelessness; irregular sleep and appetite patterns; lethargy; disinterest in previously enjoyed activities; excessive irritability and restlessness; suicidal thoughts; and inability to concentrate. Depression often occurs in the presence of one or more other disorders. For example, depression is reported to be at a higher rate in people with chronic obstructive pulmonary disease (COPD) than in the general population. COPD is a disease in which the lungs are damaged, making it difficult to breathe. Symptoms most commonly include chronic coughing and shortness of breath. A primary cause of COPD is cigarette smoking. Following a prescribed treatment plan is important for managing COPD. Unfortunately, people with COPD often do not adhere to their treatment plans. Being depressed makes adherence even more difficult. This study will evaluate the effectiveness of problem-solving therapy integrated with adherence-enhanced procedures (PSA) in treating older people with major depression and COPD. Participants in this open label study will be randomly assigned to one of two groups: PSA or PID-C. In PSA, a therapist will teach participants problem-solving strategies focusing on treatment adherence, depressive symptoms, and disability. Participants will learn behaviors and solutions to help cope with these problems. In PID-C, a therapist will teach participants to identify obstacles to treatment adherence and to discover ways to overcome them. The treatment sessions for both groups will be initiated at the inpatient Pulmonary Unit of Burke Rehabilitation Hospital and will continue in the participants' homes. All participants will receive two treatment sessions during hospitalization, eight weekly sessions following discharge, and four monthly sessions after that. While hospitalized at Burke, participants will also undergo an assessment interview for 1.5 hours and another interview for 20 minutes 2 weeks following the initial assessment. Interviews lasting 1.5 hours will also occur in the homes of the participants at Weeks 10, 14, and 26 after discharge from Burke. All assessments will focus on depression severity, level of general functioning, and COPD treatment adherence.

Interventions

BEHAVIORALProblem Solving-Rx Adherence (PSA)

In PSA, a therapist teaches the participant to identify problems related to depression, functioning, and treatment adherence; to generate multiple solutions; and to choose and implement one or more of those solutions.

BEHAVIORALPID-C

In PID-C, a therapist identifies obstacles to treatment adherence and helps the participant overcome those obstacles.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* Meets American Thoracic Society criteria for COPD * Meets DSM-IV criteria for unipolar major depression * Scores greater than 19 on 24-item Hamilton Depression Rating Scale * Fluency in English sufficient for comprehending the questionnaires of the study and for understanding the therapists

Exclusion criteria

* Unable to give informed consent * Experiencing suicidal thoughts * History of or currently meets DSM-IV criteria for the following Axis I disorders: psychotic depression, psychotic disorder, bipolar disorder, dysthymic disorder, obsessive compulsive disorder, or current substance abuse * Meets DSM-IV criteria for Axis II diagnosis of antisocial personality (by SCID-P and DSM-IV) * Scores less than 24 on Mini-Mental State Exam (MMSE) or meets DSM-IV criteria for dementia * Certain illnesses (e.g., untreated thyroid or adrenal disease, pancreatic cancer, lymphoma) * Taking drugs known to cause depression (e.g., reserpine, alpha-methyl-dopa, steroids) * Current involvement in psychotherapy * Requires nursing home placement after discharge

Design outcomes

Primary

MeasureTime frame
Depressive symptomsMeasured at week 26

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026