Impact of PharmaTE Trial on Glycemic Control, Diabetes Knowledge, Medication Adherence and Quality of Life in Type 2 Diabetes Patients: A Mixed-Method Study Protocol

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorRabia Hussain

About this trial

The goal of this clinical trial is to find out whether a pharmacist-led tele-educational program (PharmaTE trial) can help people with type 2 diabetes manage their condition better.

The main questions this study aims to answer are:

1. Does the PharmaTE trial improve blood sugar control (HbA1c levels)? 2. Does it help patients better understand their condition? 3. Does it increase how well patients follow their medication schedule? 4. Does it improve the quality of life for patients with type 2 diabetes? 5. Is this type of tele-education program feasible and acceptable for patients?

Participants will:

Be randomly placed into one of two groups:

Intervention group: Receive five virtual education sessions with a clinical pharmacist over the phone or via Zoom (each lasting 20-30 minutes), in addition to their usual diabetes care.

Control group: Continue receiving standard diabetes care from their healthcare team without the additional pharmacist-led sessions.

Complete assessments at the beginning and end of the study. These include:

A blood test for HbA1c

, Questionnaires on diabetes knowledge, medication adherence, and quality of life

Some participants in the intervention group will be invited for interviews after the sessions to share their experiences and opinions about the program.

Who can join? Adults aged 18-65 with uncontrolled type 2 diabetes (HbA1c \> 7%), receiving care at Ibrahim Bin Hamad Obaidullah Hospital in Ras Al-Khaimah, who speak Arabic and can provide consent.

Eligibility criteria

Qualifiers

Patients diagnosed with uncontrolled type 2 diabetes (defined as glycated haemoglobin [HbA1c] >7%) within the previous 12 months

Adults (18 to 65 years) of either gender

Prescribed at least one antidiabetic medication

Have access to either a telephone or a mobile phone

Disqualifiers

Under 18 years old

Pregnant ladies

Patients admitted to the emergency department

Patients with severe hepatic or renal dysfunction

Trial design

Treatments tested in this trial

  • PharmaTE Trial

Treatment groups

154 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Rabia Hussain

Lead sponsor

Universiti Sains Malaysia

Sponsor institution

Universiti Sains Malaysia

Collaborator