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Early Telemedicine Training in Patients With COPD

Not Applicable
Completed
Conditions
Chronic Obstructive Pulmonary Disease (COPD)
Interventions
Other: Telemedicine training and counselling
Registration Number
NCT02085187
Lead Sponsor
Odense University Hospital
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
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.
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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.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Telemedicine training and counsellingTelemedicine training and counselling-
Primary Outcome Measures
NameTimeMethod
Timed Up & Go test (TUG)Up to 3 weeks

Measuring 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

Clinical COPD Questionnaire (CCQ)Up to 3 weeks

A self-administered validated questionnaire measuring the health status of patients with COPD.

The five time sit to stand test (FTSST)Up to 3 weeks

Measures functional lower limb muscle strength, where the time in seconds (2 decimals) used for 5 times rising from a chair is measured.

Need for acute contact to the general practitionerUp to 3 weeks
Patient subjective perceptionUp to 3 weeks

The 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 weeks

This 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 weeks

Estimated 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 weeks

The 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.

Patients' falls during trainingUp to 3 weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Odense University Hospital

🇩🇰

Odense, Denmark

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