Adjusting to Chronic Conditions Using Education Support and Skills

NCT00727155 | Completed

• 1 other identifier: H23264
• Study Type: interventional
• Target: 3
• Locations: 1 country
• Sites: 1

Brief Summary

Medically ill patients with Congestive Heart Failure (CHF) and Chronic Obstructive Pulmonary Disease (COPD) are at increased risk for developing symptoms of anxiety and depression and are among the least frequent users of mental health services and treatments. To address the needs of chronically ill patients, we created a time-limited psychosocial intervention to maximize treatment benefits and improve the efficiency and ability of mental health care practitioners to provide services within medical care settings. This study is separated into two randomized study groups. The first group of participants will receive the ACCESS intervention immediately. The second group of participants will be followed for a period of 6 months. After a period of 6 months, those who continue to have symptoms of depression and/or anxiety will be offered the ACCESS intervention.

Conditions

Anxiety; Depression

Outcome Measures

Primary Outcomes (1)

• Beck Depression Inventory, State Trait Anxiety Inventory, SF-36 Health Survey

  Weeks 1 (baseline), 2, 4, 6, 8, 12, 24, and 36

Study Arms (2)

1

EXPERIMENTAL

Treatment

Behavioral: Adjusting to Chronic Conditions Using Education Support and Skills

2

NO INTERVENTION

Waitlist

Interventions

Adjusting to Chronic Conditions Using Education Support and Skills BEHAVIORAL

This psychosocial intervention uses a combination of cognitive-behavioral therapy and disease self-management techniques.

1

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age 18+;
• Confirmation of CHF or COPD diagnosis according to medical chart review;
• Ongoing symptoms of functional limitations due to CHF (NYHA classification of II , III, or IV as obtained by telephone interview) or COPD (Score of 3 or greater on the Medical Research Council Dyspnoea Scale \[MRC\] as obtained by telephone interview);
• Eligible patients must have clinically significant symptoms of either anxiety and/or depression as measured using patient self report questionnaires. Clinical cutoff scores for depression will be based on the Beck Depression Inventory - Second Edition (scores of 14 or more) while anxiety cutoffs will be determined using the State-Trait Anxiety Inventory - trait subscale (score of 40 or greater);
• Eligible patients will be English-speaking, as this intervention has not yet been translated to any other language.

You may not qualify if:

• History of substance abuse, bipolar disorder, psychosis or active suicidal intent (obtained from standardized structured clinical interview);
• NYHA class I, or MRC levels 1 and 2. Class 1 CHF patients and Level 1 and 2 COPD patients (by definition) will have no significantly limiting CHF or COPD symptoms. This information will be obtained through patient self-report of CHF and COPD symptoms;
• Mental status examination score in the cognitively impaired range on an established 6-item screen;
• Inability to provide informed consent or severe physical limitations restricting completion of the study protocol (e.g. vision, hearing, or physical functioning);
• Non-English speaking patients will be excluded from participation, as this intervention has not yet been translated to any other language.

Sponsors & Collaborators

• US Department of Veterans Affairs: lead

Study Sites (1)

Houston VA Medical Center

Houston, Texas, 77030, United States

Location

Related Publications (1)

• Cully JA, Stanley MA, Deswal A, Hanania NA, Phillips LL, Kunik ME. Cognitive-behavioral therapy for chronic cardiopulmonary conditions: preliminary outcomes from an open trial. Prim Care Companion J Clin Psychiatry. 2010;12(4):PCC.09m00896. doi: 10.4088/PCC.09m00896blu.

  PMID: 21085552 DERIVED

MeSH Terms

Conditions

Anxiety Disorders; Depression

Condition Hierarchy (Ancestors)

Mental Disorders; Behavioral Symptoms; Behavior

Study Officials

• Jeffrey Cully, PhD MEd

  Michael E. DeBakey VA Medical Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: FED

Study Record Dates

• First Submitted: July 29, 2008
• First Posted: August 1, 2008
• Study Start: September 1, 2008
• Primary Completion: March 1, 2009
• Study Completion: March 1, 2009
• Last Updated: July 10, 2009

Record last verified: 2009-07

Locations

US (1)