Chronic Obstructive Pulmonary Disease, Congestive Heart Failure, Diabetes, Pneumonia
Conditions
Brief summary
This study aims to assess the effectiveness of a social incentive-based gamification intervention to increase physical activity in the 3 months after hospital discharge.
Detailed description
This study aims to assess the effectiveness of a social incentive-based gamification intervention to increase physical activity in the 3 months after hospital discharge. To do this, the investigators will conduct a two-arm randomized, controlled trial during the 3-months after hospital discharge comparing a control group that uses a wearable device to track physical activity to an intervention group that uses the same wearable devices and receives a supportive social incentive-based gamification intervention to adhere to a step goal program. Patients will be enrolled during hospitalization from medicine and oncology floors into three phases. In phase 1 (hospitalization), patients inpatient step counts will be monitored. In phase 2 (week 1 post-discharge), patients will have a baseline step count estimated. In phase 3 (weeks 2-13 post-discharge), patients will be randomly assigned to the control or intervention group. Patients will be considered enrolled in the trial if they complete the run-in periods (phases 1 and 2) and then are randomized into phase 3. The enrollment phase will be part of another randomized trial which evaluates the impact of three recruitment strategies on patient enrollment. This trial will be completed and unmasked to patients before they begin the phase 1 of our study. The investigators will also explore patients' physical activity while in the hospital and if that differs across floors that have or have not deployed a nursing mobility protocol. Changes in patient functional decline and 30-day hospital readmission will also be explored.
Interventions
BEHAVIORALSocial Incentive
Participants in the intervention arm will receive social incentives as part of the intervention. See arm descriptions for more detail.
Sponsors
University of Pennsylvania
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age 18 or older * Admitted to medicine or oncology floor in the hospital
Exclusion criteria
* Inability to provide informed consent * Does not have daily access to a smartphone compatible with the wearable device * Already enrolled in another physical activity program * Inpatient mobility score of 0 or 1 indicating that physical activity is not appropriate for the patient * Any other medical conditions that would prohibit participation in a 3-month physical activity program * Unable to complete the run-in phases (e.g. not discharged from the hospital within 60 days of enrolling; not willing to use the wearable device for the 3-month post-discharge intervention).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in mean daily step count from the baseline period to the intervention period, using a wearable pedometer (Nokia Steel) to measure step count. | 13 weeks | The primary outcome variable is the change in mean daily step count from the baseline period (week 1 post-discharge) to the intervention period (weeks 2-13 post-discharge). This will be measured using the Nokia Steel wearable device. . |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| 30-day hospital readmission post-discharge, using the state's hospital database | 13 weeks | A secondary outcome variable is 30-day hospital readmission post-discharge, which will be obtained from the state-based registry. |
| Functional decline from admission to 3 months post-discharge, measured using validated survey assessments. | 13 weeks | A secondary outcome variable is functional decline from admission to 3 months post-discharge, which will be obtained from information collected through validated survey assessments. |
Countries
United States
Outcome results
None listed