Empowering Patients With Diabetes and Their Family Members: Assessing the Impact of Free Informative Mobile Messages

American University of Beirut Medical Center

Status: Not yet enrolling

Conditions: Diabetes Mellitus

Treatments: Diagnostic Test: Educational Text Messages

Study type: Interventional

Funder types: Other

Identifiers

NCT06176495

SBS-2023-0225

Details and patient eligibility

About

This is a Randomized Control Trial aiming at investigating the feasibility and effectiveness of a WhatsApp-based informative intervention on Diabetes Mellitus care in Lebanon and exploring the impact of this intervention on various aspects of Diabetes management and patient outcomes.

Family member caregivers will be also included in this interventional study as the research investigators opt to evaluate their DM related knowledge, personal health practices, their involvement in the care of patients with diabetes, and their impact on the patients' diabetes control before and after the intervention.

Full description

Participants with diabetes will be equally and randomly divided into an intervention group (patients with diabetes and their designated family member) of individualized WhatsApp groups which will include each participant individually and the study coordinator to protect their privacy; regular, 4-5 diabetes educational messages a week for a total of 12 weeks will be sent by noon (around 12 pm) to the intervention group participants. The other group, control group, will receive no text messages throughout this period. After 3 months, participants of the intervention group (patients with diabetes and their family members) will be asked to fill in a postintervention knowledge and practices questionnaire to delineate any marked differences in the context of knowledge and health behaviors. All participants with diabetes of both groups will be asked to recheck the previously noted clinical and laboratory parameters at 12 weeks to evaluate for any changes particularly among the intervention group who will also be asked to fill out a postintervention survey. After 6 months, all patients with diabetes will be asked to recheck their clinical and laboratory values again and members of the intervention group will be asked to fill in the practices section questionnaire again.

This research will additionally include Family Members of patients with diabetes who are involved in their care (cooking, aiding in management, securing/delivering medications, etc.). Family Member Caregivers of participants will be designated/noted by the participants who have diabetes themselves, and they will be included in the study based on their willingness to take part of the study. They will also be sorted into either a control or an intervention group in accordance with which group their relative with diabetes was sorted into, for example, if the patient with diabetes will be designated to be a part of the intervention group, this means that the family member caregiver participant will also be allocated to the intervention group. Our aim is to evaluate their DM related knowledge, personal health practices, their involvement in the care of patients with diabetes, and their impact on the patients' diabetes control before and after the intervention.

One point to note as well is that to ensure equality among groups and for the benefit of the control group participants, the research investigators will be sharing with them the content of the text messages originally shared with the participants of the intervention group by the End of the study.

Enrollment: 200 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Participants with Diabetes:

• Adult patients 18 years or older
• Patients with an established DM diagnosis
• Patients with a recent HbA1c level with no recent changes in treatment regimen
• Recent HbA1c > 7 but less than 9
• Patients who are on oral antidiabetic medications or basal insulin (intermediate, long acting, ultra long acting insulin)
• Patients who are adherents to the American University of Beirut Health Insurance Plan (AUB-HIP)
• Patients who have visited the Family Medicine Primary Care Clinics at American University of Beirut Clinics in the past 12 months.
• Patients with smart mobile phones and/or access to WhatsApp services
• Patients who can speak and read Arabic or English or live with someone who can read for them
• Patients with available family members involved in their care (e.g. cooking, aiding in management, securing/delivering medications, having the patient medically insured, etc.).
• Willingness to participate in the study

Exclusion Criteria for participants with Diabetes:

• Young patients below 18 years
• Patients who are on non basal insulin/bolus therapy
• Adults with cognitive impairment
• Adults with functional dependence and no assisting family member or caregiver
• Pregnant and Postpartum patients
• Patients with terminal or critical diseases (e.g., cancer; advanced heart, lung, liver, and kidney disease; Human immunodeficiency virus infection and Acquired immune deficiency syndrome and etc.)
• Patients with severe hearing or visual impairment
• Patients who can't read or have difficulty reading and do not live with someone who can read for them
• Patients who will have any of their medications modified throughout the study process will be excluded from the study as well
• Patients with a positive depression (PHQ 2) and/or anxiety (GAD 2) screening results who will be asked to follow up with their primary physician

Inclusion Criteria for Family Member Caregivers:

• Age 18 years or older
• Designated or selected by the participating patient with diabetes.
• Not diagnosed with DM
• Can read and write
• No visual or hearing impairments
• Involved in the participant's diabetes or general care and has an influence on the participant's lifestyle behaviors or medical insurance (e.g. cooking, aiding in management, securing/delivering medications, having the patient medically insured, etc.).
• Access to the WhatsApp service
• Willingness to participate in the study

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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200 participants in 2 patient groups

Control Group

No Intervention group

Description:

Patients with Diabetes and Family Member Caregivers who will receive no text messages over the designated period of the designated

Intervention Group

Other group

Description:

Patients with Diabetes and Family Member Caregivers who will receive Educational Text Messages via WhatsApp over the designated period of the intervention

Treatment:

Diagnostic Test: Educational Text Messages