Pilot Study of Changing Exercise and Physical Activity Behavior in Asthma Patients
- Conditions
- Asthma
- Interventions
- Behavioral: Group 1Behavioral: Group 3Behavioral: Group 2
- Registration Number
- NCT00227162
- Lead Sponsor
- Weill Medical College of Cornell University
- Brief Summary
The objective of this pilot study is to assess the feasibility and the potential differential impact of a novel intervention of induced positive affect and self-affirmation to increase physical activity in asthma patients.
- Detailed Description
The goals of this pilot study are to empirically test different interventional approaches to induce positive affect and self-affirmation. At the start of the study all patients in conjunction with their physicians will select a program of mild to moderate physical activity or exercise to be adopted and maintained on a routine basis. Patients also will complete the Paffenbarger Physical Activity and Exercise Index. Patients then will be divided into four groups according to the intervention they receive: 1) positive affect; 2) self-affirmation; 3) positive affect and self-affirmation; 4) control. The main outcome is the change in the Paffenbarger Physical Activity and Exercise Index scores from enrollment to 4 weeks.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- Patients will be eligible for this study if their physicians consider them medically able to participate, if they are 18 years of age or older, and if they have a diagnosis of mild to moderate asthma based on the NHLBI Asthma Expert Panel's classification system which rates symptoms, frequency of exacerbations, nocturnal attacks, activity restriction, use of medications, and pulmonary function.
Patients will be excluded from this study for the following reasons:
- If they are unable to walk several blocks for whatever reason;
- If they have musculoskeletal or neurological deficits that preclude increased physical activity;
- If they have other pulmonary diseases;
- If they have cardiac disease or other severe comorbidity;
- If they are unable to provide informed consent because of cognitive deficits;
- If they refuse to participate.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Group 1 Group 1 Positive affect Group 3 Group 3 Positive Affect and self-affirmation Group 2 Group 2 Self-Affirmation
- Primary Outcome Measures
Name Time Method Change in Paffenbarger Physical Activity and Exercise Index scores from enrollment to 4 weeks. 1-2 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
New York Presbyterian Hospital-Weill Medical College of Cornell University
🇺🇸New York, New York, United States