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Development of online support program for Chronic obstructive pulmonary disease patients - Feasibility study-

Development of online support program for Chronic obstructive pulmonary disease patients- Feasibility study- - Development of online support program for Chronic obstructive pulmonary disease patients- Feasibility study-

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000052798
Enrollment
10
Registered
2023-11-15
Start date
2023-06-22
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Chronic obstractive pulmonary disease

Interventions

Participants measure their temperature, pulse rate and transcutaneous oxygen saturation at home by using an electronic thermometer and pulse oximeter. In addition, the COPD assessment score, the pre

Sponsors

National College of Nursing, Japan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Those who have been diagnosed with chronic obstructive pulmonary disease (COPD) by a physician. (2) COPD is the main cause of the disease and physical co-morbidities do not affect ADLs. 3) Shortness of breath that interferes with daily activities (mMRC 1 or higher) 4) Those with a respiratory condition that allows for a 60-minute discussion, either in person or online 5) Those whose cognitive and physical functioning is maintained and does not interfere with participation in the needs assessment survey. Those who have family members or other support persons around them even if they have declined. 6) Those who wish to have the opportunity to speak with other patients and whose attending physician has determined that the person is receptive to the current situation to the extent that he/she is able to listen to other patients.

Exclusion criteria

Exclusion criteria: (1) Persons who have been judged by their physician to be inappropriate to participate in the research (2) Patients who are terminally ill. (3) Patients whose cognitive function has declined to the extent that it is difficult to communicate with other patients, as judged by the attending physician or the resercher during normal consultation hours and during conversations. (4) Patients who have a concomitant psychiatric disorder or are being examined by a palliative care team. (5) Those who cannot read and write Japanese.

Design outcomes

Primary

MeasureTime frame
Qualitative description focusing on acceptance to videoconferencing software (Teams) and changes in awareness and behaviour as a result of self-monitoring system.

Secondary

MeasureTime frame
(i) Qualitative description about the content of self-management education needed by COPD patients. (ii) Qualitative description about self-efficacy and the process of obtaining self-management behavior for COPD patients. (iii) Scores on the questionnaire on the acceptability of the self-monitoring system, response rate (percentage of valid responses registered), transmission rate (percentage of days data were transmitted during the period), presence and nature of problems that occurred during the period. (iv) the Hospital and depression scale (HADS), the Generalised Self-Efficacy Scale (GSES) and the St' George's Respiratory Questionnaire (SGRQ)

Countries

Japan

Contacts

Public ContactMihoko Fujii

National College of Nursing, Japan Doctral program student

fujiim@d20.ncn.ac.jp042-495-2211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026