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Early Telemedicine Training in Patients With COPD

Early Telemedicine Training and Counselling After Hospitalization in Patients With Severe Chronic Obstructive Pulmonary Disease: A Feasibility Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02085187
Enrollment
50
Registered
2014-03-12
Start date
2012-01-31
Completion date
2013-01-31
Last updated
2014-03-12

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

Conditions

Chronic Obstructive Pulmonary Disease (COPD)

Keywords

Pulmonary rehabilitation, Training, Counselling, Telemedicine, Videoconference, COPD, Chronic disease, Internet.

Brief summary

Chronic obstructive pulmonary disease (COPD) is a widespread disease that can have a major impact on the lives of individuals. An essential element in the treatment of COPD is rehabilitation of which supervised training is an important part. However, not all individuals with severe COPD can participate in the rehabilitation provided by hospitals and municipal training centres due to distance to the training venues and transportation difficulties. The aim of the feasibility study was to evaluate an individualised home based training and counselling programme via video conference to patients with severe COPD after hospitalization with regard to safety, clinical outcomes, patients' perception, organisational aspects and economic aspects.

Interventions

OTHERTelemedicine training and counselling

Training and counselling by the physiotherapist consisted of 3 weekly sessions, lasting 30-45 minutes, over a 3 week period, i.e. a total of 9 supervised sessions. Heart rate and oxygen saturation were monitored during the exercise training. This included thoracic mobilization exercises, cardio training, strength training and breathing exercises. The training intensity was progressed continuously. There were 1-2 sessions with the occupational therapist, which consisted of training and counselling on energy conservation techniques. The first session was 60 minutes long and included assessment, counselling and training. This session was delivered in the second week of the intervention. The intervention concluded in the third week, with sessions of 30 minutes as required.

Sponsors

Region of Southern Denmark
CollaboratorOTHER
Odense University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* severe and very severe COPD (i.e. with an FEV1 (forced expiratory volume in 1 second) value under 50% of the predicted value, an FEV1/FVC (forced vital capacity) ratio \< 70%, MRC (Medical Research Council Dyspnoea Scale) grade 3) * ≥40 years * hospitalization with exacerbation of COPD * declined participation in the hospital based rehabilitation * participation in videoconference sessions with a nurse for one week immediately after discharge.

Exclusion criteria

* inability to communicate via telephone and computer * systolic BP \<100mm Hg * X-rays of the thorax showing abnormalities suspicious of thoracic malignancy or lobar pneumonia * a diagnosis of cancer or recurrence of cancer within the last 5 years * hospitalization with septic shock, acute myocardial infarction (AMI) or other serious medical conditions (e.g. kidney disorder) * heart failure (EF\<30%) * if the patient did not wish to participate.

Design outcomes

Primary

MeasureTime frameDescription
Clinical COPD Questionnaire (CCQ)Up to 3 weeksA self-administered validated questionnaire measuring the health status of patients with COPD.
Timed Up & Go test (TUG)Up to 3 weeksMeasuring the time in seconds (with 2 decimals), it takes a person to rise from an ordinary chair (with back and armrest), walk 3 meters, turn around and walk back to the chair and sit down again
The five time sit to stand test (FTSST)Up to 3 weeksMeasures functional lower limb muscle strength, where the time in seconds (2 decimals) used for 5 times rising from a chair is measured.
Patients' falls during trainingUp to 3 weeks
Need for acute contact to the general practitionerUp to 3 weeks
Patient subjective perceptionUp to 3 weeksThe patients submitted a postcard with information about their experience. The postcard was an open ended question and was printed with the text Dear Department of rehabilitation. My experience of training and counselling by use of the Patient briefcase was … .
Costs per patient participating in the telemedicine rehabilitationUp to 3 weeksThis included renting of the patient briefcase, establishing of a safe line for data transmission and use of hospital staff.
Reimbursement to the hospitalUp to 3 weeksEstimated as the DRG (Diagnose Related Groups) value of the rehabilitation activity similar to the payment for the activity from the regional health system (The Region of Southern Denmark) to the hospital in accordance with health care financing system).
Focus Group interviewUp to 3 weeksThe perception of the hospital staff of the telemedicine intervention programme was assessed by a focus group interview with the occupational- and physiotherapists who carried out the telemedicine rehabilitation training and thus were familiar with the programme.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026