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Clinical Trials/NCT05867511
NCT05867511
Completed
Not Applicable

A Pilot Feasibility Study to Promote Physical Activity Motivation in Cardiovascular Disease Patients

Claudio Nigg1 site in 1 country19 target enrollmentNovember 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Diseases
Sponsor
Claudio Nigg
Enrollment
19
Locations
1
Primary Endpoint
Percentage of approached patients included
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This study investigates the feasibility of an app based intervention, which uses questionnaires and personalized motivational messages to achieve change in physical activity and sedentary behaviour of cardiovascular patients. The questionnaires and messages are based on behaviour change theories, such as the transtheoretical model. The intervention will take place over eight weeks. One week before and during the last week, physical activity will be measured via accelerometers. A comprehensive questionnaire will be given before and at the end of the intervention and Feasibility measures will be evaluated at the end as well, including an optional qualitative interview with the participants.

Detailed Description

Cardiovascular diseases are the leading cause of death and disability worldwide. They are mainly caused by lifestyle risk factors, such as physical inactivity, which is also the fourth leading risk factor for mortality. Regular physical activity is crucial for the prevention and treatment of cardiovascular diseases. Nevertheless, success in achieving long-term adherence to physical activity recommendations after an acute cardiac event or even after exercise-based cardiac rehabilitation is rather low. Furthermore, even though most research has focused on physical activity, engaging in reduced amounts of sedentary behavior is also crucial, as it represents an important cardiovascular risk even after adjusting for physical activity. Health behavior change theories, such as the transtheoretical model, and empirical evidence highlight the importance of motivation and motivational factors in the behavior maintenance or change process. Thus, the main goal of the present study is to assess preliminary effectiveness of an intervention mostly based on the transtheoretical model to promote cardiovascular patients' motivation to be physically active and to engage in reduced amounts of sedentary behavior. Most intervention components will be delivered digitally to the participants' smartphones via a study specific app. Furthermore, weekly questionnaires allow the investigators' to individualize the intervention components and investigate associations not only between-subjects, but also within-subjects over time, which is essential and has been neglected in the literature. The primary objective is to assess study feasibility.

Registry
clinicaltrials.gov
Start Date
November 1, 2022
End Date
July 31, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Claudio Nigg
Responsible Party
Sponsor Investigator
Principal Investigator

Claudio Nigg

Prof. Dr. Claudio Nigg

University of Bern

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Percentage of approached patients included

Time Frame: Approx. 5 Months

The goal is to include at least 10% of approached patients.

Completion of study assessments

Time Frame: Participants may fill out study questionnaires weekly during the 8-week intervention or not.

The goal is that, on average participants complete at least 4 out of 9 of the questionnaires of the study. Excluding dropouts.

Dropout rate

Time Frame: Participants can dropout at any time during the study (during 9 weeks for each participant)

The goal is that the dropout rate is lower than 50%

Secondary Outcomes

  • Overall satisfaction(Last questionnaire of the study for each participant (post questionnaire right after the 8 intervention weeks; 9 weeks after study start))
  • Self-efficacy(Weekly right before, during and right after the 8-week intervention for each participant.)
  • Affect(Weekly right before, during and right after the 8-week intervention for each participant.)
  • Usability(Last questionnaire of the study for each participant (post questionnaire right after the 8 intervention weeks; 9 weeks after study start))
  • Needs assessment(Last questionnaire of the study for each participant (post questionnaire right after the 8 intervention weeks; 9 weeks after study start))
  • Processes of change(Weekly right before, during and right after the 8-week intervention for each participant.)
  • Temptation(Weekly right before, during and right after the 8-week intervention for each participant.)
  • Motivation(Weekly right before, during and right after the 8-week intervention for each participant.)
  • Stage of change(Weekly right before, during and right after the 8-week intervention for each participant.)
  • Habit(Weekly right before, during and right after the 8-week intervention for each participant.)
  • Physical activity(Self-report: Weekly right before, during and right after the 8-week intervention. Device-based: during the 8 days before and the last 7 days of the intervention.)
  • Sedentary behaviour(Self-report: Weekly right before, during and right after the 8-week intervention. Device-based: during the 8 days before and the last 7 days of the intervention.)
  • Engagement(Last questionnaire of the study for each participant (post questionnaire right after the 8 intervention weeks; 9 weeks after study start))
  • Satisfaction with the specific intervention components(Last questionnaire of the study for each participant (post questionnaire right after the 8 intervention weeks; 9 weeks after study start))
  • Decisional balance(Weekly right before, during and right after the 8-week intervention for each participant.)
  • Social support(Weekly right before, during and right after the 8-week intervention for each participant.)
  • Self reported health-related quality of life(Weekly right before, during and right after the 8-week intervention for each participant.)

Study Sites (1)

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