Trial Outcomes & Findings for Med-alert Bracelet in Chronic Kidney Disease (NCT NCT00883389)

NCT ID: NCT00883389

Last Updated: 2019-11-04

Results Overview

Qualitative questionnaire with primary assessment: "How useful do you think the Med-alert device will be for future healthcare". Response recorded based on a Likert scale with response of 0 = not useful, 1 = somewhat useful, 2 = extremely useful

Recruitment status

COMPLETED

Target enrollment

26 participants

Primary outcome timeframe

3 months

Results posted on

2019-11-04

Participant Flow

Medical records of renal patients screened for eligibility upon arrival of their clinic appointment. Patients meeting study criteria approached at the end of their appointment regarding their interest in participating

All recruited participants assigned to receive intervention (medical alert accessory)

Participant milestones

Participant milestones
Measure
Med-alert Bracelet Pilot Group
All participants assigned to the medical alert accessory group. There is no placebo
Overall Study
STARTED
26
Overall Study
COMPLETED
26
Overall Study
NOT COMPLETED
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Med-alert Bracelet in Chronic Kidney Disease

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Med-alert Bracelet Pilot Group
n=26 Participants
All participants assigned to the medical alert accessory group. There is no placebo
Age, Categorical
<=18 years
0 Participants
n=5 Participants
Age, Categorical
Between 18 and 65 years
8 Participants
n=5 Participants
Age, Categorical
>=65 years
18 Participants
n=5 Participants
Age, Continuous
65.4 years
STANDARD_DEVIATION 13.8 • n=5 Participants
Sex: Female, Male
Female
13 Participants
n=5 Participants
Sex: Female, Male
Male
13 Participants
n=5 Participants
Region of Enrollment
United States
26 participants
n=5 Participants

PRIMARY outcome

Timeframe: 3 months

Qualitative questionnaire with primary assessment: "How useful do you think the Med-alert device will be for future healthcare". Response recorded based on a Likert scale with response of 0 = not useful, 1 = somewhat useful, 2 = extremely useful

Outcome measures

Outcome measures
Measure
Med-alert Pilot Group
n=24 Participants
Participants in pilot study assigned a med-alert device of bracelet or necklace
Qualitative Survey Assessmentof Perceived Usefulness of the Med-alert Device.
1 Likert scale
Interval 1.0 to 2.0

Adverse Events

Med-alert Bracelet Pilot Group

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

Dr. Jeffrey C. Fink, Associate Professor, Nephrology

University of Maryland, School of Medicine

Phone: 410-328-5720

Results disclosure agreements

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