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Medication AdherenceNCT01755312

The Effect of Medication Reminder Technology on Medication Adherence and Hypertension Outcomes

A study testing Medication reminder in people with Medication Adherence and Blood Pressure, run by Purdue University at 1 site in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

This study to evaluates how a med reminder affects the patient's ability to take medications as prescribed Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Medication Adherence, Blood Pressure
What is being tested?
Medication reminder
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
28 participants
Where
1 siteUnited States
Study dates
Jun 2013to Jan 2015
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • poor medication adherence
  • high blood pressure

Who cannot join

  • -

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Purdue University

    West Lafayette, Indiana, 47906

Other trials in United States

About this study

Official title: The Effect of Medication Reminder Technology on Medication Adherence and Hypertension

This study to evaluates how a med reminder affects the patient's ability to take medications as prescribed

Being tested
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.

  • Medication reminderDevice

    Medication reminder

Study groups in NCT01755312
Study groupRoleWhat they receive
medication reminderExperimentalmedication reminder
Receives: Device: Medication reminder
PlaceboPlacebo comparatorPlacebo

What is being measured

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

  1. self-reported medication adherence using the Morisky 8-Item Medication Adherence Scale(MMAS-8) tool

    Measured: 6 months

Secondary outcomes (1)
  1. systolic blood pressure in mmHg using a valid automated device

    Measured: 6 months

Timeline

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

  1. First posted24 Dec 2012 (estimated)
  2. Study startJun 2013
  3. Primary completionJan 2015
  4. Study completionJan 2015

Why it stopped: Research site no longer available

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
None (open label)
Enrolment
28 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01755312
Sponsor's protocol ID
2r44ago39178-02 (1208012596)
Status last verified
Aug 2015
First submitted
18 Dec 2012
Last updated
27 Aug 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Medication reminder in people with Medication Adherence and Blood Pressure, run by Purdue University at 1 site in United States.

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 2 inclusion and 1 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: stopped early, as of the sponsor's last update on 27 Aug 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. 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 was stopped early (reason given: Research site no longer available). Results are not available in the source record.

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?

self-reported medication adherence using the Morisky 8-Item Medication Adherence Scale(MMAS-8) tool (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 27 Aug 2015.

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