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Written Disclosure Therapy for Anxiety and Stress in Patients With Chronic Lung Disease

Pulmonary Therapy and Supplemental Written Disclosure Therapy for Chronic Lung Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00911794
Enrollment
66
Registered
2009-06-02
Start date
2007-01-31
Completion date
2009-03-31
Last updated
2009-06-02

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

Conditions

Chronic Lung Diseases, COPD, Pulmonary Fibrosis

Keywords

Dyspnea, Written Disclosure Therapy, COPD, Pulmonary Fibrosis, Chronic Lung Diseases, Pulmonary Rehabilitation

Brief summary

The purpose of this study is to determine whether Written Disclosure Therapy (WDT) is of any benefit to patients with chronic lung diseases who are participating in pulmonary rehabilitation.

Detailed description

Chronic lung diseases are typically associated with impaired quality of life, stress, and anxiety. Written disclosure therapy (WDT) reduces stress in patients with a variety of chronic illnesses. We sought to determine if written disclosure therapy benefits patients with chronic lung diseases when it is added as a component to the pulmonary rehabilitation program.

Interventions

OTHERDisclosure Writing (Written Disclosure Therapy)

Patients write about a stressful life experience

OTHERNeutral (Sham) Writing

Patients write about neutral subjects

Sponsors

Stony Wold-Herbert Fund, Inc.
CollaboratorOTHER
Winthrop University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of COPD or Pulmonary Fibrosis * First time participants in Pulmonary Rehabilitation program

Exclusion criteria

* Dementia * Prior significant psychiatric illness * Inability to complete the questionnaires * Inability cooperate with spirometry * Inability or to participate in outpatient follow-up over the six-month

Design outcomes

Primary

MeasureTime frame
Dyspnea and quality of lifeTwo-month and six-month time

Secondary

MeasureTime frame
Six-minute walk distanceTwo-month and six-month time
Spirometry values (FEV1 and FVC)Two-month and six-month time

Outcome results

None listed

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