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Telerehabilitation Approaches in Chronic Obstructive Pulmonary Patients

Comparison of the Effectiveness of Different Telerehabilitation Approaches in Chronic Obstructive Pulmonary Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04694729
Enrollment
54
Registered
2021-01-05
Start date
2021-01-01
Completion date
2021-12-31
Last updated
2021-01-06

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

Conditions

COPD, Telerehabilitation

Brief summary

Pulmonary rehabilitation (PR) is a first-line management strategy in chronic obstructive pulmonary patients (COPD) as it reduces shortness of breath, increases exercise capacity, and improves health-related quality of life. However, 8-50% of patients referred to PR do not participate at all, while 10-32% of those who start do not complete the program. Barriers to participation and completion include difficulty in accessing the program, poor mobility, lack of transport, and travel costs. Telerehabilitation is defined as the provision of rehabilitation services through telecommunication technology, including telephone, internet and video conference communications between the patient and the healthcare provider. Different technologies (from phone to video conferencing) have been tested in patients with COPD to enhance daily activities, exercise training and walking prescription. All of them showed positive effects on exercise tolerance, dyspnea, physical activity and quality of life. However, there is no study about which telerehabilitation program is more effective on COPD patients. The aim of this study is to investigate which telerehabilitation approach is more effective in COPD.

Interventions

OTHERvideoconference-based

Exercises will be done 3 days a week for 6 weeks, with the help of a physiotherapist via video conference.

The exercise video will be sent to the patients and they will do it 3 days a week for 6 weeks. The subjects will be asked to keep an exercise diary and the status of the diaries will be followed by calling once a week.

Sponsors

Saglik Bilimleri Universitesi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Being diagnosed with COPD (FEV1 / FVC \<70% in the stable phase of the disease) * Age \> 18 years old * Have the ability to use a smartphone

Exclusion criteria

* Musculoskeletal disorders that limit exercise * Dizziness, significant sensory or motor impairments, dementia or terminal illnesses that prevent education * Serious comorbidities such as unstable heart disease, irregular diabetes, known malignant disease, any other disease that makes the patient unsuitable for participation in the study. * Incompatible patient * Severe vision or hearing impairment * Unwillingness or inability to follow the protocol * Have had a COPD exacerbation in the previous 6 weeks

Design outcomes

Primary

MeasureTime frame
6 minute walk test(6MWT)6 week
Pulmonary function testing6 week

Secondary

MeasureTime frame
30-Second Chair Stand Test6 week
Time Up and Go Test6 week
Copd Assessment Test6 week
St George's Respiratory Questionnaire6 week
Hospital Anxiety and Depression Scale6 week
Medical Research Council Scale6 week
Short Physical Performance Battery6 week
International Physical Activity Questionnaire-Short Form6 week
Static Lung Volumes6 week

Countries

Turkey (Türkiye)

Contacts

Primary ContactNursima Bulut Physiotherapist
bltnursima@gmail.com2163463636

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026