COPD Clinical Trial
Official title:
Pilot Study Evaluating the Feasibility and Potential Benefits of a Novel Approach of COPD Self-management That Includes a Phone Assessment/Reporting System (Tele-system)
| Verified date | August 2018 |
| Source | McGill University Health Center |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this project is to conduct a pilot study evaluating the feasibility and
potential benefits of a phone assessment/reporting system (tele-system) in addition to a
written action plan and nurse case manager support to improve patients' adherence to COPD
treatment in those at risk for exacerbations.
Primary objective: explore the potential benefits with respect to patient's adherence, i.e.,
prompt use of the antibiotic and/or prednisone in the event of an exacerbation, increased
adherence to maintenance medication; to increase patient's self-efficacy" in self-managing
their disease; and to use more efficiently program resources, i.e., the case-manager.
Secondary objectives:
To assess the proportion of patients who effectively self manage exacerbations by using their
COPD Action Plan
To assess self management of COPD patients with respect to the increased adherence to regular
respiratory medication, (SmartInhaler electronic monitoring);
To assess increased self-efficacy in COPD patients identifying and managing exacerbations
(baseline vs after 12 months);
To assess symptoms recovery, health status improvement, and prevention of ER visits and
hospital admissions for COPD exacerbations.
To assess the efficiency in using program resources,
To evaluate the feasibility of this treatment approach and to provide pilot data (needed for
a larger multi-centre clinical trial;
To evaluate the feasibility and need of assessment during and after exacerbation onset,
health-related quality of life and physical activity;
To evaluate the safety of this approach; this is in terms of the delay in starting prednisone
and an unfavourable outcome (ER visits and/or hospitalization).
| Status | Completed |
| Enrollment | 40 |
| Est. completion date | November 29, 2017 |
| Est. primary completion date | June 8, 2016 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 40 Years and older |
| Eligibility |
Inclusion Criteria: - Patients will be adults with COPD at high risk for exacerbations - Post bronchodilator spirometry FEV1 <80% pred. and FEV1/FVC <0.70 - Aged = 40 yrs - Smoking = 10 pack-years - 1 or more exacerbations requiring antibiotic or prednisone in the last year. (This is the population with the highest chance of having another exacerbation - Combination therapy LABA-ICS (Advair) with or without an anticholinergic (Spiriva or Atrovent) and a rescue SABA (Ventolin) Exclusion Criteria: - Combination therapy LABA-ICS other than Advair - Home oxygen for 18-24 hours/day - Chronic CO2 retention - Previous NIMV/MV - Cognitive impairment - Does not speak English or French fluently - Severe co-morbidities such as bronchiectasis with recurrent infections, severe left congestive heart failure - Survival <6 months - Any significant medical condition other than COPD that may also result in dyspnea (e.g. unstable angina, BMI > 40). |
| Country | Name | City | State |
|---|---|---|---|
| Canada | Montreal Chest Institute | Montreal | Quebec |
| Lead Sponsor | Collaborator |
|---|---|
| McGill University Health Center | GlaxoSmithKline |
Canada,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Process and Implementation Evaluation | Qualitative research is the most appropriate method to explore experiences of health care providers, practice staff, study staff and patients.39 We will conduct group and individual interviews with the case manager, physicians, nurses and staff at each site. We will also interview a random sample of patients. | end of study at 12 months | |
| Other | Covariates- Sociodemographic and clinical data | Information on age, sex, education, employment, marital status, living alone, BMI, weight/height, exacerbations, co-morbidities, and health resource utilization will be gathered from a questionnaire that patients complete at baseline. Smoking status will be queried and smokers will be classified as current, ex or never smoker as well and cumulative pack-years will be estimated. | 12 months | |
| Other | Comorbidities: | The Charlson index40;41 a widely used indicator of comorbid conditions, will be calculated for each participant. A complete list of comorbidities will be extracted by study staff at baseline from the patient's medical chart, as well as from patient recall at the baseline visit. The global score ranges from 0 to 33, highest scores indicating more comorbidities, and was shown predictive of mortality in COPD. | 12 months | |
| Other | Baseline respiratory status. Dyspnea will be evaluated using a 5-grade Medical Research Council (MRC) dyspnea scale. | Dyspnea will be evaluated using a 5-grade Medical Research Council (MRC) dyspnea scale. | 12 months | |
| Other | Spirometry will be done according to stringent standards. Disease severity is categorized according to the GOLD classification. Measures will be obtained at baseline and end of treatment by the research coordinator. | will be done according to stringent standards. Disease severity is categorized according to the GOLD classification. Measures will be obtained at baseline and end of treatment by the research coordinator. | 12 months | |
| Other | Anxiety and Depression. | The Patient Health Questionnaire-9 (PHQ-9) [Kroenke K, J Gen Intern Med 2001] will be used to assess and monitor depression, together with the Generalized Anxiety Disorder (GAD-7), a 7-item scale. The GAD-7 has also proved to have good sensitivity/specificity to screen for panic, social anxiety and post-traumatic stress disorder [Spitzer RL, Arch Intern Med 2006]. | 12 months | |
| Primary | - Patient adherence to action plan | Proportion of patients who initiate use of COPD Action Plan including starting exacerbation medications (i.e., antibiotics and/or prednisone) within 3 days. | within 3 days. | |
| Secondary | Respiratory medication adherence | Patient monitoring will be done using the SmartInhaler for Advair and Ventolin on a sample of subjects. | 12 months | |
| Secondary | Self-efficacy to manage exacerbations: | Self-efficacy will be measured using a scale from 0-10 asking patients to rate their level of confidence, 0= not confident at all, 10=very confident, based on the "Understanding COPD questionnaire" [Wilson 2007; O'Neill 2012] and the principles of self-efficacy scale design, according to the construct proposed by Bandura.Level of confidence will be rated with respect to: taking medications as prescribed; items that are behavior-specific related to recognition and appropriate management of exacerbation including ability to identify signs of deterioration and need to initiate the prescribed action plan. CAT- The COPD Assessment Test (CAT) is a simple and quick questionnaire to give a reliable measure of health status in COPD which will complement existing approaches and will assess impact of COPD and exacerbation on the health of individual patients [Jones P 2009; Jones PW 2009]. | 12 months | |
| Secondary | Health care utilization | The Exacerbation Questionnaire provides detailed information about contacts with health care providers for both respiratory and non-respiratory problems including unplanned physician visits, Emergency Department, use and hospitalizations since the previous call. Program resources: Practice staff who assist with patient identification and chart review will be paid for their time on an hourly basis. Nurse case managers will keep records of all contact with patients (content, time spent); information on interaction between the nurse case manager and other providers (physicians, pharmacists, etc.) including type of call, who is making the call, duration and reason will be recorded. | 12 months | |
| Secondary | Phone System | We will closely monitor use (according to symptom changes from the daily diary), record all feedback related to utilization (patients' responses using keypad vs. question verified when case manager call back the patient) and algorithm with corresponding status (Well, Worse, Alarm). | 12 months |
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