Physical Activity Telehealth Intervention After Percutaneous Coronary Procedures
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|ClinicalTrials.gov Identifier: NCT01673100|
Recruitment Status : Completed
First Posted : August 27, 2012
Last Update Posted : December 2, 2014
|Condition or disease||Intervention/treatment||Phase|
|Physical Activity||Behavioral: Physical Activity Promotion Intervention||Not Applicable|
|Study Type :||Interventional|
|Actual Enrollment :||50 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||Physical Activity Telehealth Intervention After Percutaneous Coronary Procedures|
|Study Start Date :||March 2011|
|Actual Primary Completion Date :||September 2014|
|Actual Study Completion Date :||September 2014|
Experimental: Physical Activity Promotion Intervention
Subjects in the experimental group (Physical Activity Promotion Telehealth Intervention) will receive messages on the study cell phone - approximately 2 to 3 messages every day. These messages will be tips to help them engage in physical activity and also to help them keep the physical activity appropriate. Walking will be primarily the suggested mode of activity.
Behavioral: Physical Activity Promotion Intervention
Subjects in the experimental group (Physical Activity Promotion Telehealth Intervention) will receive messages on the study cell phone - approximately 2 to 3 messages every day. Depending on the subject's responses to the questionnaires at baseline (stages and processes of change) they will be given tips to help them engage in physical activity (such as messages to increase their self-efficacy or confidence, walking with a friend or spouse, breaking up physical activity bouts into 10 minutes bouts, etc.) and also to help them keep the physical activity appropriate. Walking will be primarily the suggested mode of activity.
No Intervention: Atttention Control
Subjects in the attention control group will receive only general health messages on their study cell phone (not physical activity promoting messages). They also will receive any usual post-PCI procedure care that all get.
- Feasibility Aspects of the Physical Activity Telehealth Intervention [ Time Frame: 6 months ]
Evaluate the feasibility of each component of this pilot study, in order to refine the intervention for a larger clinical trial. This will include:
- Evaluate all aspects of implementation (numbers of subjects contacted, enrollment, attrition; problems and solutions identified using the telehealth platform, time for delivery; subject acceptance and perception).
- Evaluate feasibility of the data collection methods (time required for data collection, missing data, reliability estimates of outcomes).
- Estimate effect sizes for sample size determinations for a future, larger clinical trial.
- Physical Activity Measures [ Time Frame: 6 months ]
Pilot test the impact of the Physical Activity Promotion Telehealth Intervention in post-PCI patients over time compared to patients receiving attention only, on the following outcomes:
- Movement through the stages of readiness for physical activity.
- Behavior change constructs (self efficacy for exercise, decisional balance, and use of processes for change).
- Amount of physical activity (estimated energy expenditure per day as measured by the actigraph accelerometer) and exercise (reported minutes exercising per day).
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01673100
|United States, Nebraska|
|Bryan LGH Medical Center|
|Lincoln, Nebraska, United States, 68516|
|Nebraska Heart Hospital|
|Lincoln, Nebraska, United States, 68526|
|Principal Investigator:||Janet L Nieveen, PhD, RN||University of Nebraska|