Level Up: Gamification to Increase Mobility in the Hospital

Sponsor
University of Pennsylvania (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04300764
Collaborator
(none)
150
1
2
12
12.5

Study Details

Study Description

Brief Summary

Low mobility is a mediator for poor outcomes of hospital care. Wearable devices will be used and 2-way texting via patient smartphones to monitor patients' physical activity during hospitalization with and without gamification to improve patient adherence to existing guidance on recommended activity. After discharge, investigators will assess patient care utilization (SNF, inpatient vs home rehab, ED visits, readmission) and conduct validated surveys on patient function at 30 days after discharge.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Gamification Intervention
N/A

Detailed Description

Hospitalization is a common occurrence for older adults; approximately 6.8 million Medicare seniors experience an admission for acute care in any given year. This is often a sentinel event in the overall health trajectory of older adults that is complicated by functional impairment, Skilled Nursing Facility placement, and reduced mobility after discharge.

In the current paradigm, low mobility during hospitalization is largely viewed as a temporary inconvenience that should not affect overall functional ability or outcomes such nursing home placement and that patients should return to their previous activity level soon after they return home without lingering mobility changes. Recent research, however, suggests disruptions of basic activities of daily life such as mobility (getting out of bed and walking) may be "traumatic" or "toxic" to older adults with long-term post-hospital effects. What is lacked is precise data on how much immobility is noxious and how much mobility is needed to protect against adverse outcomes.

The primary objective is to assess the effectiveness of a gamification intervention to increase physical activity before hospital discharge. Investigators will explore patients' physical activity while in the hospital and if that differs across floors that have already deployed a nursing mobility protocol (Founders 10, 11, 12, 14). Investigators will also explore changes in patient functional status, SNF placement, and 30-day hospital readmission.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Health Services Research
Official Title:
Gamification to Increase Mobility in the Hospital
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Apr 30, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control

Participants will be recruited during an inpatient stay and given a Fitbit watch that will transmit data to the Way to Health study platform. Control participants' steps will be passively monitored. Data will continue to be collected for 30 days after discharge.

Experimental: Gamification Intervention

Participants will be recruited during an inpatient stay and given a Fitbit watch that will transmit data to the Way to Health study platform. Intervention patients will receive daily text messages to help them set goals, receive feedback and support on their progress towards daily goals, and receive points for daily goals achieved. Data will continue to be collected for 30 days after discharge.

Behavioral: Gamification Intervention
Intervention participants will receive daily text messages to help them set goals, receive feedback and support on their progress towards daily goals, and receive points for daily goals achieved. Each participant will be given a Fitbit watch that will transmit data to the Way to Health study platform. Data will be passively collected during the inpatient stay and for 30 days after hospital discharge.

Outcome Measures

Primary Outcome Measures

  1. Change in mean daily step count during hospitalization [Average 5 days]

    The primary outcome variable is the change in mean daily step count during hospitalization (from enrollment to discharge).

Secondary Outcome Measures

  1. Proportion of patients who attain pre-specified step thresholds during hospitalization and after discharge [Average 35 days]

    Proportion of patients in each group who attain pre-specified step thresholds of 1000, 2000, 3000 during hospitalization and 3500, 4000, 4500, and 5000 after discharge

  2. Hospital length of stay [Average 5 days]

    Length of inpatient hospital stay

  3. Discharge to post-acute facilities [30 days]

    Discharge to post-acute facilities (skilled nursing facility or rehabilitation facility)

  4. 30-day acute care utilization [30 days]

    30-day acute care utilization (hospital readmission or ED visits)

  5. Change in activities of daily living [Average 35 days]

    Change in functional status measure of activities of daily living from admission to 30 days post-discharge.using the Activities of Daily Living Scale.

  6. Change in difficulty with walking [Average 35 days]

    Change in functional status measure of difficulty with walking from admission to 30 days post-discharge using the Activities of Daily Living Scale.

  7. Change in life space assessment [Average 35 days]

    Change in functional status measure of life space assessment from admission to 30 days post-discharge.using the Life Space Activity Survey

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Admitted to a medicine or cardiology floor in the hospital

  • Age 50 years or older

  • Have an AMPAC (mobility scale) score of greater than or equal to 21 or a Braden mobility sub-scale score of 4.

Exclusion Criteria:
  • Inability to provide informed consent

  • Does not have daily access to a smartphone compatible with the wearable device and not willing to use a device that the study team can provide

  • Inpatient AMPAC score of less than 21 or a Braden mobility sub-scale score less than 4 indicating that independent physical activity may not be appropriate for the patient

  • Are already enrolled in another physical activity study

  • Any conditions that would prohibit participation in an inpatient physical activity program (at the discretion of attending physician or nurse caring for the patient in the hospital). To minimize the risk of contamination across study arms, we will only approach one patient per hospital room in shared rooms

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Pennsylvania Philadelphia Pennsylvania United States 19104

Sponsors and Collaborators

  • University of Pennsylvania

Investigators

  • Principal Investigator: Ryan Greysen, MD, MHS, MA, University of Pennsylvania

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ryan Greysen, Ryan Greysen, MD, MHS, MA, University of Pennsylvania
ClinicalTrials.gov Identifier:
NCT04300764
Other Study ID Numbers:
  • 834466
First Posted:
Mar 9, 2020
Last Update Posted:
Mar 11, 2021
Last Verified:
Mar 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 11, 2021