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Patients Take MedicineNCT02197689

A Trial for a Personalized Medication Management Platform to Improve Medication Adherence

A study testing Personalized Medication Management Platform for SMS Reminder in people with Patients Take Medicine, run by Taipei Medical University.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Taiwan has attracted much attention for its National Health Insurance (NHI) and healthcare system around the world with many countries in Europe and the United States using it as a benchmark. Read more about this study

Who is it for?
Ages 20 years and older
Conditions the study is for
Patients Take Medicine
What is being tested?
Personalized Medication Management Platform for SMS Reminder
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
763 participants
Where
No sites listed yet
Study dates
Jan 2010to Nov 2012
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Delayed or forgot to take medications over the last 3 days
  • Received a min. 7-day medication prescription
  • Able to receive SMS using mobile phones / devices
  • 20 years or older
  • Having intention to receive active treatment

Who cannot join

  • Unable to receive SMS via mobile phones
  • Illiterate and < 20 years of age
  • Received outpatient prescription drugs for ≤ 7 days
  • External use, injections and traditional Chinese medicine
  • Planned to go abroad
  • Cold, cough, or prescribed with analgesics

About this study

Official title: Mobile Intelligent Personal Medication Management Platform

Taiwan has attracted much attention for its National Health Insurance (NHI) and healthcare system around the world with many countries in Europe and the United States using it as a benchmark. However, increasing medication costs over the past two years account for more than 25% of total expenditure, surpassing every OECD member and mounting increasing pressure on the NHI. Nevertheless, patient medication adherence is relatively low. Thus, the investigators assessed the effectiveness of a personalized medication management system for improving the medication adherence for patients, in order to save long term medication costs.

Read the detailed description

Design, Setting and Patients: The investigators developed a mobile personalized medication management platform (PMMP) to reduce delayed and missed medications. The investigators conducted a randomized control trial in medical centers of northern Taiwan from January 2010 to July 2012 using 1198 participants that missed or delayed their medications during past three days. They received a minimum 7-day to 14-day maximum medication prescription.

Interventions: Patients were randomized into a control group which non-received any SMS reminder for medication using and an intervention group which received a SMS reminder everyday in mobile devices.

Primary Outcome(s) and Measure(s): The primary outcomes were compared patient medication adherence among experimental and control groups.

Being tested
Personalized Medication Management Platform for SMS Reminder
Keywords
Personalized Medication Management, Medication Adherence, SMS Medication Reminder
Medical subject headings
Medication Adherence

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Personalized Medication Management Platform for SMS ReminderDevice

    The Personalized Medication Management Platform was developed by investigators that integrated with Hospital Information System (HIS) to collect the prescription information of patients and automatically send SMS to remind

Study groups in NCT02197689
Study groupRoleWhat they receive
SMS Medication ReminderExperimental763 patients were assigned to experimental group
Receives: Device: Personalized Medication Management Platform for SMS Reminder
No SMS ReminderNo intervention435 patients were assigned to control group as no SMS reminder

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The proportion of patients in delaying and forgetting medications

    Measured: Patients who participated in this trial will be sent SMS during 7days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Jul 2014 (estimated)
  2. Study startJan 2010
  3. Primary completionJul 2012
  4. Study completionNov 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
763 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02197689
Sponsor's protocol ID
NSC 99-2218-E-038-001
Status last verified
Jun 2014
First submitted
17 Jul 2014
Last updated
23 Jul 2014
Results posted
No
Data monitoring committee
No

Publications

  • Huang CY, Nguyen PA, Clinciu DL, Hsu CK, Lu JR, Yang HC, Wu CC, Tsai WC, Chou YC, Kuo TBJ, Chang PL, Jian WS, Li YJ. A personalized medication management platform (PMMP) to improve medication adherence: A randomized control trial. Comput Methods Programs Biomed. 2017 Mar;140:275-281. doi: 10.1016/j.cmpb.2016.12.012. Epub 2016 Dec 30.

    PubMed 28254084

Questions about this trial

What is this clinical trial studying?

A study testing Personalized Medication Management Platform for SMS Reminder in people with Patients Take Medicine, run by Taipei Medical University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 23 Jul 2014. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The proportion of patients in delaying and forgetting medications (time frame: Patients who participated in this trial will be sent SMS during 7days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02197689, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jul 2014.

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