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Motivational Intervention for Asthma (MI-ACT)

Primary Purpose

Asthma

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Motivational Communication
Control
Sponsored by
Hopital du Sacre-Coeur de Montreal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma focused on measuring Adherence, Asthma Control, Asthma Quality Of Life, Motivational Communication, Motivational Interviewing

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients 18 years and older
  • Primary diagnosis of moderate-severe persistent asthma (as per GINA)
  • Prescribed inhaled corticosteroid medication (min dose of 250 µg fluticasone equivalent per day) for at least 12 consecutive months
  • Uncontrolled asthma (≥ 1.25 on the Asthma Control Questionnaire)
  • Covered by a drug insurance plan (e.g., RAMQ)
  • Non-adherent to ICS medication (based on having filled less than 50% of their prescriptions over the last year)
  • Able to speak English or French.

Exclusion Criteria:

  • Any other medical condition that confers greater illness morbidity than asthma (e.g., active cancer)
  • Severe psychopathology (e.g., schizophrenia)
  • Apparent cognitive or language deficit
  • Are or plan to become pregnant or move outside of Quebec over the course of the study.

Sites / Locations

  • Hopital du Sacre-Coeur de Montreal

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Motivational Communication

Control

Arm Description

Up to 3 x 30 minute brief MC sessions within 4-6 week period

Usual care

Outcomes

Primary Outcome Measures

Inhaled corticosteroid adherence
Inhaled corticosteroid adherence measured according to the following validated equation: # of treatment days (based on the # of canisters filled at the pharmacy x the duration of each prescription) divided by the # of prescription days (# of days the patient is expected to be taking his/her medication)

Secondary Outcome Measures

Inhaled corticosteroid adherence
Inhaled corticosteroid adherence measured according to the following validated equation: # of treatment days (based on the # of canisters filled at the pharmacy x the duration of each prescription) divided by the # of prescription days (# of days the patient is expected to be taking his/her medication)
Asthma Control Questionnaire (Juniper)
Self report measure of asthma symptoms
Asthma Control Test
Self report measures of asthma symptoms
Asthma Self-Efficacy Scale (Tobin)
Self report measure of asthma self-efficacy, i.e., perceived ability to deal with asthma
Mini Asthma Quality of Life Questionnaire (Juniper)
Self report measure of how asthma influences quality of life

Full Information

First Posted
June 21, 2011
Last Updated
March 14, 2022
Sponsor
Hopital du Sacre-Coeur de Montreal
Collaborators
Jewish General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01381159
Brief Title
Motivational Intervention for Asthma
Acronym
MI-ACT
Official Title
Motivational Intervention for Asthma Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2011 (Actual)
Primary Completion Date
August 2019 (Actual)
Study Completion Date
August 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hopital du Sacre-Coeur de Montreal
Collaborators
Jewish General Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The high burden of asthma appears to be related to poor asthma control, which is associated with more frequent asthma symptoms, greater bronchodilator use and functional impairment, and worse pulmonary function. Despite the availability of effective treatments, more than 58% of asthmatics are poorly controlled. Daily adherence to inhaled corticosteroid (ICS) regimens is considered by experts to be one of the most important behavioural factors linked to achieving optimal asthma control. However, there is a paucity of research on interventions specifically designed to improve ICS adherence among adult asthmatics. The vast majority of intervention studies to date used atheoretical interventions to target behaviour change, relying mainly upon educational approaches which have been criticised for "failing to translate knowledge into action." This may be due to the fact that most education-based approaches do not specifically address or help patients overcome ambivalence about behaviour change, which is necessary for ensuring daily adherence. Motivational communication (MC) is a client-centred intervention that focuses on enhancing intrinsic motivation to change a particular behaviour, and exploring and resolving ambivalence about behaviour change. Brief MC sessions (e.g., 1-5 x 15-30 minute sessions) have been shown to improve a variety of health behaviours (e.g., reduce alcohol consumption, improve dietary habits, increase exercise behaviour, and improve medication adherence) and health outcomes (reduce blood pressure, body mass index, and cholesterol levels). However, no studies to date have assessed the efficacy of using MC to improve ICS adherence in asthmatics. This study aims to assess the efficacy of using MC to improve daily medication (ICS) adherence in a sample of poorly controlled, non-adherent asthmatics. It is hypothesized that patients randomized to the MC condition will exhibit significantly improved ICS adherence at 6 and 12-months post-intervention, independent of baseline levels and covariates, relative to patients randomized to the usual care control condition.
Detailed Description
Background: The high burden of asthma, which affects 300 million people worldwide, appears to be related to poor asthma control, which is associated with more frequent asthma symptoms, greater bronchodilator use and functional impairment, and worse pulmonary function. The availability of effective treatments suggests that asthma can be well controlled in most patients. However, Canadian statistics reveal that over 58% of asthmatics are poorly controlled. Achieving optimal asthma control relies upon several behavioral factors, including minimizing exposure to known triggers (e.g., pets, dust, pollen) and improving health behaviors (e.g,. quitting smoking and adhering to medication). Of these, daily adherence to inhaled corticosteroid (ICS) regimens is considered by experts to be one of the most important behavioral factors linked to achieving optimal asthma control. This is because taking ICS medications as prescribed (i.e., good adherence) has been shown to be effective for achieving good asthma control even in patients who fail to adequately manage/minimize exposure to known triggers (e.g., indoor allergens, exercise). Despite the efficacy of ICS's, recent trends in adherence behaviour suggest that asthmatics are not adherent to these medications, with rates being as low as 32%, even in patients with severe asthma. Explanations range from simply forgetting to having distorted/ erroneous illness and medication beliefs. Currently, there is a paucity of research on interventions specifically designed to improve ICS adherence among adult asthmatics. Most previous work has been conducted in pediatric samples which have yielded inconsistent results that are difficult to generalize to adult samples. Of the studies conducted among adults, most suffer from important methodological limitations (e.g., small sample sizes, no intent to treat analyses, failure to control for contact time, no objective measure of adherence) that make it difficult to either generalize findings or interpret them with confidence. Most importantly, the vast majority of intervention studies to date used atheoretical interventions to target behaviour change, relying mainly upon educational approaches which have been criticised for "failing to translate knowledge into action." This may be due to the fact that most education-based approaches do not specifically address or help patients overcome ambivalence about behaviour change, which is necessary for ensuring daily adherence. Motivational communication (MC) is a client-centred intervention that focuses on enhancing intrinsic motivation to change a particular behaviour (i.e., take medication as prescribed), and exploring and resolving ambivalence about behaviour change. Brief MC sessions (e.g., 1-5 x 15-30 minute sessions) have been shown to improve a variety of health behaviours (e.g., reduce alcohol consumption, improve dietary habits, increase exercise behaviour, and improve medication adherence) and health outcomes (reduce blood pressure, body mass index, and cholesterol levels). No studies to date have assessed the efficacy of using MC to improve ICS adherence in asthmatics. Objective: The purpose of this study is to conduct a single site RCT to assess the efficacy of using MC to improve daily medication (ICS) adherence in a sample of poorly controlled, non-adherent asthmatics. A brief (3-5 x 15-30 minute sessions), manualized MC intervention was developed by our laboratory using pilot funding. This intervention is empirically-driven and uses established behavioural and motivational strategies to encourage change. Methods: 182 poorly controlled, non-adherent adult asthmatics will be recruited from the outpatient asthma clinic of Hôpital du Sacré-Coeur de Montreal (HSCM). Patients will be screened on the day of their asthma clinic visit to verify eligibility. Eligible patients consenting to have their medical and pharmacy records verified by the research team and who are identified as both having poorly controlled asthma (Asthma Control Questionnaire score ≥1.25) and being non-adherent to ICS medication (filled < 50% of their ICS medication in the last year) will be invited to participate in the study. Patients will undergo baseline assessments (pulmonary function, asthma control, self-efficacy, and quality of life) and will then be randomly assigned to a usual care + MC or usual care comparison group. This trial has been designed to conform to the CONSORT guidelines. The primary outcome measure will be ICS adherence at 12 months post-intervention, with preliminary analyses conducted at 6-months post-intervention. Adherence will be measured according to the following validated equation: # of treatment days (based on the # of canisters filled at the pharmacy x the duration of each prescription) divided by the # of prescription days (# of days the patient is expected to be taking his/her medication). Data will be obtained by accessing the patient's pharmacy records and drug insurance databases (i.e., RAMQ, reMed). Secondary outcomes include self-reported medication adherence, adherence motivation, stage of change, pulmonary function, asthma control, self-efficacy, and quality of life scores 6 & 12 months post-intervention. Impact: This will be the first appropriately designed RCT to test the impact of a brief, manualized MC intervention on asthma medication (ICS) adherence that may be easily incorporated into existing education programs and/or clinical practice and may significantly improve asthma outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Adherence, Asthma Control, Asthma Quality Of Life, Motivational Communication, Motivational Interviewing

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
58 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Motivational Communication
Arm Type
Experimental
Arm Description
Up to 3 x 30 minute brief MC sessions within 4-6 week period
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Usual care
Intervention Type
Behavioral
Intervention Name(s)
Motivational Communication
Intervention Description
Brief MC sessions focused on medication adherence within 4-6 week period
Intervention Type
Behavioral
Intervention Name(s)
Control
Intervention Description
Standard medical care
Primary Outcome Measure Information:
Title
Inhaled corticosteroid adherence
Description
Inhaled corticosteroid adherence measured according to the following validated equation: # of treatment days (based on the # of canisters filled at the pharmacy x the duration of each prescription) divided by the # of prescription days (# of days the patient is expected to be taking his/her medication)
Time Frame
12 months post-intervention
Secondary Outcome Measure Information:
Title
Inhaled corticosteroid adherence
Description
Inhaled corticosteroid adherence measured according to the following validated equation: # of treatment days (based on the # of canisters filled at the pharmacy x the duration of each prescription) divided by the # of prescription days (# of days the patient is expected to be taking his/her medication)
Time Frame
6 months post-intervention
Title
Asthma Control Questionnaire (Juniper)
Description
Self report measure of asthma symptoms
Time Frame
12 months post-intervention
Title
Asthma Control Test
Description
Self report measures of asthma symptoms
Time Frame
12 months post-intervention
Title
Asthma Self-Efficacy Scale (Tobin)
Description
Self report measure of asthma self-efficacy, i.e., perceived ability to deal with asthma
Time Frame
12 months post-intervention
Title
Mini Asthma Quality of Life Questionnaire (Juniper)
Description
Self report measure of how asthma influences quality of life
Time Frame
12 months post-intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients 18 years and older Primary diagnosis of moderate-severe persistent asthma (as per GINA) Prescribed inhaled corticosteroid medication (min dose of 250 µg fluticasone equivalent per day) for at least 12 consecutive months Uncontrolled asthma (≥ 1.25 on the Asthma Control Questionnaire) Covered by a drug insurance plan (e.g., RAMQ) Non-adherent to ICS medication (based on having filled less than 50% of their prescriptions over the last year) Able to speak English or French. Exclusion Criteria: Any other medical condition that confers greater illness morbidity than asthma (e.g., active cancer) Severe psychopathology (e.g., schizophrenia) Apparent cognitive or language deficit Are or plan to become pregnant or move outside of Quebec over the course of the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kim L Lavoie, PhD
Organizational Affiliation
Hopital du Sacre-Coeur de Montreal
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Simon L Bacon, PhD
Organizational Affiliation
Hopital du Sacre-Coeur de Montreal
Official's Role
Study Chair
Facility Information:
Facility Name
Hopital du Sacre-Coeur de Montreal
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4J 1C5
Country
Canada

12. IPD Sharing Statement

Links:
URL
http://mbmc-cmcm.ca
Description
Website of the research lab
URL
http://mbmc-cmcm.ca/project/motivational-interviewing-for-asthma-adherence-and-control-a-randomized-controlled-trial/
Description
Study website

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Motivational Intervention for Asthma

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