Trial Outcomes & Findings for Improving Medication Adherence Through Graphically Enhanced Interventions in Acute Coronary Syndromes (NCT NCT00399880)

NCT ID: NCT00399880

Last Updated: 2017-09-25

Results Overview

Validated self-report measure of medication adherence. Possible range 12-48, with lower values indicating better adherence.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

130 participants

Primary outcome timeframe

Approximately 2 weeks after hospital discharge

Results posted on

2017-09-25

Participant Flow

Participant milestones

Participant milestones
Measure
Health Literacy Intervention
Illustrated medication schedules, pill boxes, pharmacist counseling Health literacy intervention: Illustrated medication schedules, pill boxes, pharmacist counseling
Usual Care
Usual care arm
Overall Study
STARTED
65
65
Overall Study
COMPLETED
65
65
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Improving Medication Adherence Through Graphically Enhanced Interventions in Acute Coronary Syndromes

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Health Literacy Intervention
n=65 Participants
Illustrated medication schedules, pill boxes, pharmacist counseling Health literacy intervention: Illustrated medication schedules, pill boxes, pharmacist counseling
Usual Care
n=65 Participants
Usual care arm
Total
n=130 Participants
Total of all reporting groups
Age, Continuous
52.6 years
STANDARD_DEVIATION 9.2 • n=5 Participants
52.2 years
STANDARD_DEVIATION 10.7 • n=7 Participants
52.4 years
STANDARD_DEVIATION 9.9 • n=5 Participants
Sex: Female, Male
Female
27 Participants
n=5 Participants
29 Participants
n=7 Participants
56 Participants
n=5 Participants
Sex: Female, Male
Male
38 Participants
n=5 Participants
36 Participants
n=7 Participants
74 Participants
n=5 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 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
62 Participants
n=5 Participants
63 Participants
n=7 Participants
125 Participants
n=5 Participants
Race (NIH/OMB)
White
2 Participants
n=5 Participants
2 Participants
n=7 Participants
4 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
1 Participants
n=5 Participants
0 Participants
n=7 Participants
1 Participants
n=5 Participants
Income
<$10,000
40 Participants
n=5 Participants
44 Participants
n=7 Participants
84 Participants
n=5 Participants
Income
$10,000-$20,000
18 Participants
n=5 Participants
12 Participants
n=7 Participants
30 Participants
n=5 Participants
Income
>$20,000
5 Participants
n=5 Participants
5 Participants
n=7 Participants
10 Participants
n=5 Participants
Income
Missing
2 Participants
n=5 Participants
4 Participants
n=7 Participants
6 Participants
n=5 Participants
Employment status
Unemployed
31 Participants
n=5 Participants
20 Participants
n=7 Participants
51 Participants
n=5 Participants
Employment status
Full-time
5 Participants
n=5 Participants
4 Participants
n=7 Participants
9 Participants
n=5 Participants
Employment status
Part-time
3 Participants
n=5 Participants
4 Participants
n=7 Participants
7 Participants
n=5 Participants
Employment status
Other (disabled, retired)
24 Participants
n=5 Participants
36 Participants
n=7 Participants
60 Participants
n=5 Participants
Employment status
Missing
2 Participants
n=5 Participants
1 Participants
n=7 Participants
3 Participants
n=5 Participants
Education
11.6 years
STANDARD_DEVIATION 3.0 • n=5 Participants
11.5 years
STANDARD_DEVIATION 2.9 • n=7 Participants
11.6 years
STANDARD_DEVIATION 2.9 • n=5 Participants
Rapid Estimate of Adult Literacy in Medicine (REALM)
41.1 units on a scale
STANDARD_DEVIATION 21.7 • n=5 Participants
39.1 units on a scale
STANDARD_DEVIATION 22.7 • n=7 Participants
40.1 units on a scale
STANDARD_DEVIATION 22.1 • n=5 Participants
Smoking status
Never
18 Participants
n=5 Participants
29 Participants
n=7 Participants
47 Participants
n=5 Participants
Smoking status
Former
14 Participants
n=5 Participants
5 Participants
n=7 Participants
19 Participants
n=5 Participants
Smoking status
Current
33 Participants
n=5 Participants
28 Participants
n=7 Participants
61 Participants
n=5 Participants
Smoking status
Missing
0 Participants
n=5 Participants
3 Participants
n=7 Participants
3 Participants
n=5 Participants

PRIMARY outcome

Timeframe: Approximately 2 weeks after hospital discharge

Population: Participants who were able to be contacted and provided outcome data.

Validated self-report measure of medication adherence. Possible range 12-48, with lower values indicating better adherence.

Outcome measures

Outcome measures
Measure
Health Literacy Intervention
n=38 Participants
Illustrated medication schedules, pill boxes, pharmacist counseling Health literacy intervention: Illustrated medication schedules, pill boxes, pharmacist counseling
Usual Care
n=38 Participants
Usual care arm
Adherence to Refills and Medications Scale (ARMS)
12.03 units on a scale
Standard Deviation 2.59
12.18 units on a scale
Standard Deviation 3.81

SECONDARY outcome

Timeframe: Approximately 2 weeks after hospital discharge

Population: Participants who were able to be contacted and provided outcome data.

Validated measure of confidence in taking medications correctly. Possible range 13-39, with higher values indicating greater confidence.

Outcome measures

Outcome measures
Measure
Health Literacy Intervention
n=39 Participants
Illustrated medication schedules, pill boxes, pharmacist counseling Health literacy intervention: Illustrated medication schedules, pill boxes, pharmacist counseling
Usual Care
n=42 Participants
Usual care arm
Self-Efficacy for Appropriate Medication Use Scale (SEAMS)
32.8 units on a scale
Standard Deviation 4.8
31.5 units on a scale
Standard Deviation 6.7

Adverse Events

Health Literacy Intervention

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

Usual Care

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

Kathryn Goggins, Research Coordinator

Vanderbilt University Medical Center

Phone: 6159364819

Results disclosure agreements

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