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Effectiveness of a diabetic self-management education intervention through WhatsApp for people with type 2 diabetes: A randomised controlled feasibility study

Not Applicable
Conditions
Type 2 Diabetes
Metabolic and Endocrine - Diabetes
Registration Number
ACTRN12621001672842
Lead Sponsor
The University of Newcastle
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
90
Inclusion Criteria

•Males or females diagnosed with T2DM and regularly followed up at the diabetic centres.
•Male or female aged 18 to 60 years old.
•HbA1C greater than 9 % (Universally considered poor control)
•Patients are willing to participate in the study and have the capacity to provide informed consent.
•Agree to follow the study procedures
•Can Speak and read Arabic
•Can to access and use WhatsApp

Exclusion Criteria

•People with T1DM or gestational diabetes
•People who have participated in any other clinical trial.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Self-efficacy assessed by using UK-Diabetic Management Self-Efficacy Scale (UK-DMSES)'[UK-DMSES will assessed at baseline, immediately post-intervention (at 8th week), and 3 months post-intervention completion];Diabetic knowledge assessed by using Diabetic Knowledge Test (DKT)[DKT will assessed at baseline, immediately post-intervention (at 8th week ), and 3 months post-intervention completion]
Secondary Outcome Measures
NameTimeMethod
HbA1c assessed by blood test [HbA1c will assessed at baseline, immediately post-intervention (at 8th week), and 3 months post-intervention completion.];Anxiety and Depression assessed by using Hospital Anxiety and Depression Scale (HADS)[HADS will assessed at baseline, immediately post-intervention (at 8th week ), and 3 months post-intervention completion];Quality of life assessed by using Diabetes Management Quality of Life (DMQOL)[DMQOL will assessed at baseline, immediately post-intervention (at 8th week ), and 3 months post-intervention completion]
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