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Trial of Asthma Patient Education (TAPE)

Trial of Asthma Patient Education (TAPE)

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00148408
Enrollment
600
Registered
2005-09-08
Start date
2003-12-31
Completion date
2005-12-31
Last updated
2010-04-30

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

Conditions

Asthma

Keywords

Asthma, Placebo, Education

Brief summary

The purpose of this research study is to investigate the way that educational approaches and presentation of a drug may affect the response to montelukast and placebo (an inactive medication) in subjects with asthma.

Detailed description

This is a study of the effects of education and drug presentation on efficacy of montelukast and placebo in asthma. This trial will answer the following questions: 1) Is there a true placebo response in asthma that is not due to non-specific factors? 2) Can the placebo effect in asthma be augmented by interventions that increase expectancy of benefit? 3) Can interventions that increase expectancy augment the effect of active treatment? 4) Are placebo effects additive or interactive with treatment effects?

Interventions

DRUGMontelukast
BEHAVIORALEducation

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
American Lung Association Asthma Clinical Research Centers
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age 15 or older * physician diagnosed asthma * regular use of prescribed asthma medication over preceding year * post-bronchodilator FEV1 of at least 75% of predicted * inadequate asthma control over preceding two months

Exclusion criteria

* current or past smoking (greater than 10 pack-years) * serious asthma exacerbation within previous three months * regular use of oral corticosteroids * history of respiratory failure due to asthma * current use of montelukast or history of adverse reaction to montelukast * concomitant interfering medical condition * participation in another clinical trial * inability or unwillingness to perform study procedures * pregnancy, lack of effective contraception (when appropriate), lactation

Design outcomes

Primary

MeasureTime frame
Morning peak expiratory flow

Secondary

MeasureTime frame
Asthma diaries
Asthma questionnaires (Asthma Control Score, Asthma Symptom Utility Index, Asthma Quality of Life)
Spirometry
Shortness of Breath Questionnaire
Adherence monitoring
Generic health quality of life (SF-36)

Countries

United States

Outcome results

None listed

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