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Behavioral Intervention

Web-Based Intervention for COPD

Aurora, CO
N/A
Waitlist Available
Research Sponsored by University of Colorado, Denver
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Has been diagnosed with COPD and is being seen at the ECHCS VA Medical Center or the University of Colorado Pulmonology clinics
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 0 months, 3 months
Awards & highlights
No Placebo-Only Group

Summary

This trial offers different levels of emotional and behavioral support for people adjusting to living with COPD. The support is provided by experienced social workers and overseen by the primary investigator.

See full description
Who is the study for?
This trial is for individuals living with Chronic Obstructive Pulmonary Disease (COPD). Specific eligibility criteria are not provided, but typically participants would need a confirmed diagnosis of COPD and be stable enough to engage in the intervention.Check my eligibility
What is being tested?
The study is testing a web-based whole health support system designed for people with COPD. It's narrative-based, tiered, and offers psychosocial and behavioral support by licensed clinical social workers under supervision.See study design
What are the potential side effects?
Since this intervention involves psychosocial and behavioral support rather than medication or medical procedures, traditional side effects are not expected. However, emotional discomfort due to discussing personal issues may occur.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I have COPD and am a patient at ECHCS VA or University of Colorado Pulmonology.
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Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~0 months, 3 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 0 months, 3 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Personal Health Questionnaire- 9 item (PHQ9)
Secondary study objectives
Generalized Anxiety Disorder-7 items (GAD7)
Other study objectives
St George Respiratory Questionnaire (SGRQ)

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Participant led tiered interventionExperimental Treatment1 Intervention
Participants living with COPD will navigate to the website and choose the tiered intervention that fits their needs. The first tier is information about COPD only. Second tier is reflective writing prompts for illness narrative generation and the third tier is asynchronous mental health support from a licensed clinical social worker.

Find a Location

Closest Location:University of Colorado Anschutz Medical Campus· Aurora, CO

Who is running the clinical trial?

University of Colorado, DenverLead Sponsor
1,841 Previous Clinical Trials
3,028,522 Total Patients Enrolled
~40 spots leftby Aug 2028