Trial Outcomes & Findings for Smart Television and Exercise Promotion for Independent Living Facilities (NCT NCT03001778)

NCT ID: NCT03001778

Last Updated: 2018-09-20

Results Overview

Ten likert-type questions assessing user-friendliness of technology. Each question has five answer options that range from "Strongly Agree" to "Strongly Disagree". Scores range from 0-100. A score of 68 or above is considered above average. All scores averaged.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

67 participants

Primary outcome timeframe

After 1 hour usability session

Results posted on

2018-09-20

Participant Flow

Participant milestones

Participant milestones
Measure
Community Residents
Community prototype testing Usability Testing: Usability testing of "ready made" workouts.
ILF Resident Usability Testing
ILF Prototype testing Usability Testing: Usability testing of "ready made" workouts.
Overall Study
STARTED
21
46
Overall Study
COMPLETED
21
46
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Smart Television and Exercise Promotion for Independent Living Facilities

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Community Usability Testing
n=21 Participants
Prototype testing Usability Testing: Usability testing of "ready made" workouts in a group format.
ILF Usability Testing
n=46 Participants
Prototype testing Usability Testing: Usability testing of "ready made" workouts in as an individual.
Total
n=67 Participants
Total of all reporting groups
Age, Continuous
NA years
STANDARD_DEVIATION NA • n=5 Participants
NA years
STANDARD_DEVIATION NA • n=7 Participants
NA years
STANDARD_DEVIATION NA • n=5 Participants
Sex: Female, Male
Female
8 Participants
n=5 Participants
33 Participants
n=7 Participants
41 Participants
n=5 Participants
Sex: Female, Male
Male
13 Participants
n=5 Participants
13 Participants
n=7 Participants
26 Participants
n=5 Participants
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants
n=5 Participants
0 Participants
n=7 Participants
1 Participants
n=5 Participants
Race (NIH/OMB)
Asian
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Black or African American
1 Participants
n=5 Participants
0 Participants
n=7 Participants
1 Participants
n=5 Participants
Race (NIH/OMB)
White
19 Participants
n=5 Participants
45 Participants
n=7 Participants
64 Participants
n=5 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=5 Participants
1 Participants
n=7 Participants
1 Participants
n=5 Participants
Region of Enrollment
United States
21 participants
n=5 Participants
46 participants
n=7 Participants
67 participants
n=5 Participants

PRIMARY outcome

Timeframe: After 1 hour usability session

Ten likert-type questions assessing user-friendliness of technology. Each question has five answer options that range from "Strongly Agree" to "Strongly Disagree". Scores range from 0-100. A score of 68 or above is considered above average. All scores averaged.

Outcome measures

Outcome measures
Measure
Community Residents
n=21 Participants
Community prototype testing Usability Testing: Usability testing of "ready made" workouts.
ILF Resident Usability Testing
n=46 Participants
ILF Prototype testing Usability Testing: Usability testing of "ready made" workouts.
System Usability Scale (SUS)
73.57 units on a scale
Standard Deviation 22.12
74.70 units on a scale
Standard Deviation 13.94

Adverse Events

Community Usability Testing

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

ILF Usability Testing

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Valerie Myers, PhD

Klein Buendel

Phone: 3035654343

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place