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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05667363
Other study ID # 2022-HX-43
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 20, 2022
Est. completion date September 1, 2023

Study information

Verified date December 2022
Source China-Japan Friendship Hospital
Contact Ting Yang, MD
Phone 84206272
Email zryyyangting@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Digital Therapeutics (DTx) is an evidence-based,clinically evaluated software to treat,manage,and prevent a broad spectrum of diseases and disorders according to Digital Therapeutics Alliance,which may improve the adherence of patients with chronic obstructive pulmonary disease (COPD) to use inhaled medication and reduce the risk of acute exacerbation. This study plans to carry out a randomized controlled trial (RCT), using digital therapy to record and manage the behavior data of patients with COPD in the process of using inhaler medication, and analyze the correlation between digital therapy of COPD and patients' drug compliance and treatment effect.


Description:

Chronic obstructive pulmonary disease (COPD) is a major disease that causes death and disability worldwide. The World Health Organization (WHO) estimates that COPD has become the third leading cause of death worldwide, accounting for 6% of the global total deaths in 2019. COPD seriously affects the quality of life of patients and causes heavy economic burden to society and families. Inhaled medication is the key treatment for COPD, and the adherence of inhaled medication is closely related to the effect of disease control. Studies have shown that incorrect and irregular use of metered-dose inhaler are very common in patients.Previous studies have shown that patients using mobile phones to record respiratory symptom diaries, and send blood oxygen saturation, heart rate, body temperature and other data, as well as changes in medication and medical treatment to the portal, and doctors access the data online to identify potential acute exacerbation and take intervention measures, can reduce the risk of acute exacerbation of COPD. The digital therapeutics of COPD consists of patient mobile phone program, doctor management software and intelligent medication recorder. It develops a digital intervention plan for patients, helping patients intuitively and comprehensively understand the treatment plan and how to act through medication tracking reminder. It also helps doctors to view visualized patient medication, symptoms and other trend data online to understand the real treatment response of patients. This study take digital therapeutics as intervention to explore the correlation between digital therapy and patient medication adherence and treatment effect.


Recruitment information / eligibility

Status Recruiting
Enrollment 582
Est. completion date September 1, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: 1. Fully understand and willing to sign the written informed consent; 2. Local residents diagnosed COPD by physician; 3. Aged 40 and above; 4. Plan to receive metered-dose inhaler as long-term treatment; 5. Have a smartphone and can apply WeChat applet after training; Exclusion Criteria: 1. Certain comorbidities (e.g. unstable coronary complications); 2. Undergone thoracic, abdominal or ophthalmic surgery in recent 3 months; 3. Pregnant or lactating women; 4. ABS allergy history.

Study Design


Related Conditions & MeSH terms


Intervention

Combination Product:
Digital Intervention
Digital therapeutics are consist of a smartphone app and an intelligent medication recorder. The intelligent medication recorder can automatically record medication using data and reminds patients through the app. Patients can also record their symptom on the app for doctors to monitor.

Locations

Country Name City State
China China-Japan Friendship hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
China-Japan Friendship Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of adherent patients. The proportion of patients whose TAI scores 50. 24 weeks
Secondary Average times of AECOPD The average times of self-reported history of AECOPD since the last follow-up 4, 12 ,24 weeks
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