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Intervention StudyNCT03182972

Intervention Study on Medication Reconciliation Among Pharmacists in Two Tertiary Hospitals in Nigeria

A study testing Medication reconciliation in people with Intervention Study, run by University of Ibadan at 2 sites in Nigeria.

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

This study will assess the current practice of medication reconciliation among pharmacists in the selected institutions with a view to making an intervention to address gaps discovered Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Intervention Study
What is being tested?
Medication reconciliation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,000 participants
Where
2 sitesNigeria
Study dates
2 Aug 2016to 30 Apr 2019
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
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Participant has diabetes and/or hypertension
  • Registered pharmacists in the selected institutions

Who cannot join

  • Participants that are neither diabetic nor hypertensive
  • Unregistered pharmacists in the selected institutions

Trial locations and contacts

2 sites in 1 country.

Nigeria2 sites
  • University College Hospital

    Ibadan, Oyo State, 2334

  • University of Ilorin Teaching Hospital

    Ilorin, Kwara State

Other trials in Nigeria

About this study

This study will assess the current practice of medication reconciliation among pharmacists in the selected institutions with a view to making an intervention to address gaps discovered

Read the detailed description

Background information garnering will be done among the pharmacists in the two selected hospitals to collect data on current practice of medication reconciliation. Focus group discussion will be done in the intervention group so as to identify peculiarities of their practice and to provide the best approach to carrying out the intervention. Diabetes and hypertensive patients in medical outpatient clinic will be interviewed in order to assess current practice of medication reconciliation.

Intervention will be channeled towards addressing gaps discovered. University College Hospital, Ibadan, Oyo State will be the intervention group, while University of Ilorin Teaching Hospital, Kwara State will be the control group.

The effect of the intervention will be measured over time to ensure that medication reconciliation is implemented in the selected institutions.

Being tested
Medication reconciliation
Keywords
intervention study, medication reconciliation, pharmacists, Nigeria, Diabetes, Hypertension
Medical subject headings
Diabetes Mellitus, Hypertension

What participants receive

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

  • Medication reconciliationOther

    Pre-post intervention

Study groups in NCT03182972
Study groupRoleWhat they receive
Intervention armExperimentalSeminar presentation will be done using the followings: 1. Power point presentation on the following topics as it relates to medication reconciliation: 1. Communication skill (with patients and also with other members of the healthcare team) 2. Documentation of pharmaceutical care activities 3. Medication history taking 4. Drug therapy problems 5. Medication reconciliation practice 2. Case studies on medication reconciliation 3. Role plays on medication reconciliation
Receives: Other: Medication reconciliation
Control armNo interventionControl group

What is being measured

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

  1. Medication reconciliation: Percentage unreconciled medications

    Percentage unreconciled medications

    Measured: 3 months

Timeline

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

  1. First posted9 Jun 2017
  2. Study start2 Aug 2016
  3. Primary completion30 Apr 2019
  4. Study completion30 Apr 2019

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
Model description
University College Hospital, Ibadan will serve as the intervention group while University of Ilorin Teaching Hospital, Ilorin will serve as the control group.
Masking
Double blind
Who is masked
Participant, Care provider
Enrolment
1,000 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03182972
Sponsor's protocol ID
MR/UCH/FMC/73247
Status last verified
Nov 2022
First submitted
8 Jun 2017
Last updated
30 Nov 2022
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

A study testing Medication reconciliation in people with Intervention Study, run by University of Ibadan at 2 sites in Nigeria.

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 2 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 30 Nov 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Nigeria. 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. 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?

Medication reconciliation: Percentage unreconciled medications (time frame: 3 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 30 Nov 2022.

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