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Managing Risk Factors for Chronic Diseases through Online Consultations: A Clinical Study

Effectiveness of Teleconsultation Package on Physiological Risk Factors of Preventable Non-Communicable Diseases among Indonesian Adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240608062042N2
Enrollment
72
Registered
2025-05-02
Start date
2025-02-18
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Indonesian Adults.

Interventions

Intervention 1: The intervention group will engage in a nine-week program that will include teleconsultations and educational materials (videos and posters) focused on physical activity and nutrition.

Sponsors

Universitas Muhammadiyah Surabaya
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: Indonesian adults aged 40 to 60 years. At risk of or currently managing preventable non-communicable diseases (NCDs) such as hypertension, diabetes, or obesity. Access to the necessary technology (e.g., smartphone, internet) to engage in teleconsultations. Ability to understand and communicate in the language used for the teleconsultation. Willingness to comply with the study protocols and interventions.

Exclusion criteria

Exclusion criteria: Pregnant women. Individuals with severe chronic conditions such as advanced heart disease or end-stage renal disease. Individuals with severe mental health disorders. Individuals who have undergone major surgery within the last six months. Participants currently undergoing treatment for cancer or other major non-communicable diseases. Individuals without access to necessary technology (e.g., smartphone, internet). Individuals with language barriers. Individuals with a history of non-compliance in previous studies. Participants currently enrolled in other clinical trials or studies that might interfere with the outcomes of this study.

Design outcomes

Primary

MeasureTime frame
1.Blood Pressure (BP); 2.Fasting Blood Sugar (FBS); 3.Blood Total Cholesterol (Chol); 4.Blood Uric Acid (UA); 5.Body Weight (BW); 6.Waist-to-Hip Ratio (WHR); 7.Peripheral Blood Oxygen (SpO2); 8.Dietary Intake; 9.Frequency of Physical Activity. Timepoint: before intervention and 12, 24 weeks after intervention. Method of measurement: 1. Blood Pressure (BP): Sphygmomanometer; 2. Fasting Blood Sugar (FBS): 3-in-1 Glucose, Uric Acid, and Cholesterol Measurement Tool; 3. Blood Total Cholesterol (Chol): 3-in-1 Glucose, Uric Acid, and Cholesterol Measurement Tool; 4. Blood Uric Acid (UA): 3-in-1 Glucose, Uric Acid, and Cholesterol Measurement Tool; 5. Body Weight (BW): Digital Scale; 6. Waist-to-Hip Ratio (WHR): Measurement Tape; 7. Peripheral Blood Oxygen (SpO2): Pulse Oximeter; 8. Dietary Intake: SQFFQ (Semi-Quantitative Food Frequency Questionnaire); 9. Frequency of Physical Activity: IPAQ (International Physical Activity Questionnaire).

Secondary

MeasureTime frame
E-Health Literacy. Timepoint: before intervention and 12, 24 weeks after intervention. Method of measurement: eHealth Literacy Scale (e-HEALS).

Countries

Indonesia

Contacts

Public ContactArdalan Shariat

Tehran University of Medical Sciences

ardalansh2002@gmail.com+98 21 8896 5909

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026