Efficacy of Mobile Phone Short Message Service (SMS) Reminder and Consultation on Asthma Control

NCT02189616 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 360

Last updated 2014-08-19

No results posted yet for this study

Summary

Asthma is the disease being studied. The main objective of this study is to assess the clinical efficacy of mobile phone short message service (SMS) reminder and consultation on the self-management and outcomes of poorly controlled asthma which is first diagnosed in a time period of 3 months. The secondary objective is to explore the cost-benefit and cost-effectiveness of the proposed intervention.

Aims: The main aim of this study is to assist asthma patients to practice asthma self-management at home by sending reminders and responding to patients' consultations with mobile phone short message service (SMS), which will eventually help them to control their asthma, and prevent asthma exacerbation. Thus, the ultimate goal of this proposed study is to improve patient health outcome via enhancing patient-physician interaction through mobile phone short message service (SMS) that is low-cost and could be followed easily by the patients and their physicians.

The hypothesis is that asthma patients who receive weekly text message reminders to educate them and reinforce adherence will have better asthma outcome, such as asthma control, while the intervention integrating patient consultation and reminders by SMS improve asthma outcome even more. The investigators further hypothesize that these subjects under intervention will have an improvement in secondary measures including quality of life and patient satisfaction. The investigators also anticipate that such an approach in asthma management will be cost-effective.

Conditions

Interventions

BEHAVIORAL

SMS reminder

send weekly mobile phone short message reminders to the intervention group

OTHER

SMS consultation

told patients to consult qualified asthma nurses by SMS when they need

OTHER

regular care

patients are asked to fill in their paper asthma diary daily for 3 months

Sponsors & Collaborators

  • Baoji Central Hospital

    collaborator OTHER
  • Hanzhong Central Hospital

    collaborator OTHER
  • Yan'an University Affiliated Hospital

    collaborator OTHER
  • Xijing Hospital

    lead OTHER

Principal Investigators

  • liqiang song, doctor · first affiliated hospital, the fourth military medical university

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2014-12-31
Completion
2014-12-31

Countries

  • China

Study Locations

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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 NCT02189616 on ClinicalTrials.gov