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Usability Study of IeHS in Indonesia

NCT04179344 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2019-11-27

No results posted yet for this study

Summary

Technology that has a particular focus on patients' needs and ease-of-use and -access plays a significant role in the development of e-health and m-health. The proposed model of a secured mobile health application may promote patient's self-management and enhances adherence in chronic therapy exactly as it is easy-to-use, reducing patient's burden in accessing medication information and instructions, and providing the opportunity for direct communications with health providers in charge for each patient with access to mobile technologies. Consequently, medication errors and unnecessary paperwork in the healthcare system will be avoided as well as giving more time for healthcare providers to pay greater attention to delivering medical care effectively and efficiently.

Conditions

  • Human Immunodeficiency Virus
  • Tuberculosis
  • Interpersonal Relations
  • Mobile Phone Use
  • Adult

Interventions

OTHER

Integrated e-healthcare services (IeHS) web-based app

Each participant is asked to complete study tasks using the IeHS web-based app as a part of IeHS simulation. This activity is followed by user experience survey, and an in-depth interview to explore user satisfaction on the IeHS web-based app

Sponsors & Collaborators

  • University of Groningen

    collaborator OTHER

  • Bekasi City Public Hospital

    lead OTHER

Principal Investigators

  • Lusiana R Idrus, Master · Bekasi City Public Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-08-05
Primary Completion
2019-10-31
Completion
2019-10-31

Countries

  • Indonesia

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04179344 on ClinicalTrials.gov