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Improving access to care of non communicable diseases in Tribal population dominated areas of Madhya Pradesh through use of mobile health and teleheath based interventions

Improving access to care for chronic noncommunicable diseases using digital health interventions in selected tribal population dominated districts of Madhya Pradesh – a mixed-methods implementation research study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058947
Enrollment
720
Registered
2023-10-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: I60-I69- Cerebrovascular diseases Health Condition 2: J40-J47- Chronic lower respiratory diseases Health Condition 3: E08-E13- Diabetes mellitus Health Condition 4: I10- Essential (primary) hypertension Health Condition 5: I20-I25- Ischemic heart diseases Health Condition 6: C50-C50- Malignant neoplasms of breast Health Condition 7: C51-C58- Malignant neoplasms of female genital organs Health Condition 8: C00-C14- Malignant neoplasms of lip, oral cavity and pharynx Health Con

Interventions

Intervention1: digital health intervention package: Sending medication & appointment reminders, disease management and lifestyle related queries, health messages, training of peripheral workers. Dur

Sponsors

ICMR New delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age 30 years and above 2. Having an established documented chronic NCD and taking treatment 3. Living in the study area for at least six months 4. Either owning a mobile phone themselves or having at least one member of their family living in the same household owning a mobile phone. 5. Having at least one member of their family living in the same household being able to read Hindi or English 6. Consenting to participate in the study

Exclusion criteria

Exclusion criteria: There is no exclusion criteria

Design outcomes

Primary

MeasureTime frame
1.change in adherence to medication 2. Regularity in visits of patients for consultation of NCD to health centres 3.Frequency of contact with peripheral health worker and intervention providersTimepoint: For all three primary outcomes - Baseline data collection starts o months ( starting of 2nd year of project) Follow up data- after 12 months—

Secondary

MeasureTime frame
change in – - CVD risk score - Measures of adiposity - BMI, Weight, Waist hip ratio, Waist circumference - Physical activity levels, healthy dietary practices, tobacco and alcohol use - Knowledge of disease complications and preventive steps - Patients health related quality of life and satisfaction Implementation outcomes – - Reach - AdoptionTimepoint: Follow up data for secondary outcomes will be collected 12 months after the initiation of the trial (baseline data collection)—

Countries

India

Contacts

Public ContactDr Anindo Majumdar

AIIMS Bhopal

anindo.cfm@aiimsbhopal.edu.in9487635186

Outcome results

None listed

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