Automated Oxygen Titration at Home in Patients With COPD on Home Oxygen — DaiLiHOT_2  

COPD Clinical Trial

Official title: Automated Oxygen Titration in Daily Life of Patients With Chronic Obstructive Pulmonary Disease on Home Oxygen Treatment

Status Completed

Clinical Trial Summary

Twelwe patients with COPD and long term oxygen treatment (LTOT) will be included in the study. An automated home oxygen titrations (HOT) device will be attached to the patient´s home oxygen equipment. For 2x4 consequent days, the patients will be monitored and saturations, oxygen flow and physical activity level will be registered. In randomized order, the patients will use their usual fixed oxygen dose or automated oxygen titration during the first four days and then crossover. The monitoring consists of a wrist pulse oximeter (register pulse and saturation which is send to the HOT device) and a physical activity sensor attached to the patient's knee. At study start and after both of the four days the patients´dyspnea and QoL will be assessed. After the study period the patients will in an explorative design based on qualitative methodology be interviewed in order to explore the patients experiences with automated oxygen titration during daily activity and on dyspnea.

Clinical Trial Description

Twelve patients with COPD and long term oxygen treatment (LTOT) will be included in the study. The purpose is to evaluate the feasibility of automated oxygen titration during daily living incl. activities. The pilot feasibility design has been chosen as this will be - the first study testing automated oxygen titration in the patients' home, - the first study testing automated oxygen titration adjusted not only at rest but during the entire day with the possibility to deliver up to 8 l/min. Demographic data, will be registered. Oxygen consumption and oxygen saturation (SpO2) will be registered. O2matic Home Oxygen Treatment (HOT) is a device, which based on continuous, non-invasive measurement of SpO2 adjusts oxygen flow to the patient within a defined target interval. SpO2-target can be set individually, but in this study will be fixed at 90 to 94 % with a flow from 0.5-8 l/min. If SpO2 falls below 90 % oxygen flow will increase, and if SpO2 increases above 94 % oxygen flow will decrease. The adjustments are done every second based on average SpO2 for the last 15 seconds. Blood gas analysis (ABG): Two venous blood sample will be taken, the first with the usual oxygen dose and the second after 20 minutes with an oxygen flow of 8 l/min. The analysis will look at pH-value and the PvCO2. Clinical COPD Questionnaire (CCQ): 24-hour CCQ measures health status and can be used to assess health-related quality of life (HRQL). It measures symptoms within the last 24 hours as well as functional and mental state, and it is a predictor of mortality in patients with COPD. It is a short questionnaire with 10 items rated on a scale with 6 grades. The items are dyspnea at rest and on exercise, fear of worsening in the condition, depression, cough and sputum, limitations with strenuous and moderate physical activity, limitations with daily activities and social activities. Besides the total score ranging from 0 to 6 there are 3 subscores representing symptoms, mental state and functional state. An improvement of 0.4 is considered clinically significant. CCQ is validated in several languages including danish, and has proven to have good reliability and validity and to be responsive to changes and interventions, such as exacerbations, pulmonary rehabilitation and smoking cessation. Physical Activity Level: The physical activity will be monitored using A SENS motion® sensor. With a patch above the knee, SENS registers time at rest, standing, walking, steps taken and motion intensity. 600 steps per day has been suggested to be a clinically relevant difference for patients with COPD. Intervention An O2matic HOT device will be attached to the patient´s home oxygen equipment. For 2x4 consequent days, the patients will be monitored and saturations, oxygen flow and physical activity level will be registered. In randomized order, the patients will use their usual fixed oxygen dose or automated oxygen titration during the first four days and then crossover. The monitoring consists of a wrist pulse oximeter (register pulse and saturation) and a physical activity sensor attached to the patient's knee. At study start and after both of the four days the patients will be assessed using the CCQ. Baseline visit 1. The patients will be asked to meet for a baseline testing at the hospital. Besides gathering information, two venous blood gases will be taken. The first with the usual oxygen dose and the next after 20 minutes of 8 l/min. The blood sample will be analyzed in order to avoid respiratory acidosis at home (the patients will be excluded if the develop hypercapnia according the exclusion criteria). 2. The randomization will be performed, and the SENS monitor will be attached above the knee. 3. An appointment will be made for a home visit depending on the order of the randomization. The home visits will be made by the primary investigator 4. The patients will be followed for 2x4 days. Four days with usual fixed oxygen dose and four days with automated oxygen titration. In a "non- pilot" design CCQ could be a primary outcome, which would require 42 patients to show a MCID of 0.4 with a standard deviation = 0.9. A convenience sample of 12 patients is chosen in the present study, as we consider 12 patients to give a clear impression on the use of HOT at home and also a high enough number of patients to gather data on differences on SpO2 interval, CCQ and the activities performed by the patients, well knowing that we cannot expect to detect a difference with high probability. Continuous variables are examined for normality and analyzed with either paired t-test (in case of normality) or Wilcoxon-signed-rank test (in case of non-normality). IBM SPSS Statistics for Windows, ver. 25.0 will be used for all statistical analyses. ;

Related Conditions & MeSH terms

• COPD
• Hypoxemia
• Hypoxia

• NCT number: NCT05556187
• Study type: Interventional
• Source: Hvidovre University Hospital
• Status: Completed
• Phase: N/A
• Start date: January 10, 2023
• Completion date: December 29, 2023