Quality of sleep of 24 COPD patients Respiratory Chronic Obstructive Pulmonary Disease (COPD)
Conditions
Interventions
24 volunteer COPD sufferers: 12 live/12 placebo.
Sponsors
SOE Health Ltd
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. COPD 2. Volunteers attached to Rivergreen Medical Centre
Exclusion criteria
Exclusion criteria: 1. Non-COPD sufferers 2. Not attached to Rivergreen Medical Centre 3. Not adults
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Improved quality of sleep for COPD sufferers | — |
Secondary
| Measure | Time frame |
|---|---|
| Recorded fortnightly at clinic: 1. Recording blood pressure 2. Blood oxygen saturation (blood sats) 3. Forced Vital Capacity (FVC) 4. Forced Expiratory Volume in one second (FEV1) Recorded at start and end of trial at clinic: 5. St George's quality of life/sleep questionnaire | — |
Countries
United Kingdom
Contacts
Public ContactNeil Stentiford
Outcome results
None listed