Effectiveness and Implementation of the Assessment of Burden of Chronic Conditions (ABCC)-Tool
Primary Purpose
Chronic Obstructive Pulmonary Disease, Asthma, Diabetes Mellitus, Type 2
Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Assessment of Burden of Chronic Conditions (ABCC)-tool
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease
Eligibility Criteria
Inclusion Criteria:
- diagnosis COPD, asthma, Diabetes Mellitus type 2 and/or heart failure
- can understand and read the Dutch language
Exclusion Criteria:
- COPD or asthma: used prednisone due to an exacerbation less than six weeks ago
- Heart failure or diabetes mellitus type 2: hospitalized less than six weeks ago
- Healthcare providers or patients who have already used the Assessment of Burden of COPD-tool are excluded from the control group
- Patients who have already used the Assessment of Burden of COPD-tool will be excluded from the intervention group
Sites / Locations
- Maastricht University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
ABCC-tool
Usual care
Arm Description
The intervention group will use the ABCC-tool during consultation with their healthcare provider. Healthcare providers in the intervention group will receive a short instructional film about the ABCC-tool before the start of the study. Additionally, healthcare providers from 12 practices will be invited for interviews, evaluating the context and process of implementation.
The control group will receive usual care, and healthcare providers will not be instructed
Outcomes
Primary Outcome Measures
Perceived quality of care (PACIC): Patient Assessment of Chronic Illness Care
Measured with the Patient Assessment of Chronic Illness Care, for total group. The scale has 20 items. Answers range from 1 to 5. Average scores (range 1-5) will be calculated. Higher scores mean more frequent presence of the aspect of structured chronic care.
Secondary Outcome Measures
Perceived quality of care (PACIC): Patient Assessment of Chronic Illness Care
Measured with the Patient Assessment of Chronic Illness Care, for total group and for each condition separately. The scale has 20 items. Answers range from 1 to 5. Average scores (range 1-5) will be calculated. Higher scores mean more frequent presence of the aspect of structured chronic care.
Perceived quality of care (PACIC): Patient Assessment of Chronic Illness Care
Measured with the Patient Assessment of Chronic Illness Care, for each condition separately. The scale has 20 items. Answers range from 1 to 5. Average scores (range 1-5) will be calculated. Higher scores mean more frequent presence of the aspect of structured chronic care.
Quality of life (EQ-5D-5L)
Measured with the EuroQol-5D-5L, for total group and for each condition separately. The scale consists of the EQ-5D-5L descriptive system with 5 questions, and a VAS-scale. Answers range from 1 (best) to 5 (worst). EQ-5D-5L health states, defined by the EQ-5D-5L descriptive system, will be converted into a single index value (Dutch values). The EQ-5D-5L VAS will also be determined.
Capability well-being (ICECAP-A)
Measured with the ICEpop CAPability measure for Adults, for total group and for each condition separately. The questionnaire consists of 5 questions. Answers range from 1 (no capability) to 4 (full capability for an attribute). A tariff value for an overall state can be calculated by summing the values across the individual attributes. This code will allow calculation of ICECAP-A tariffs for each respondent in a study
Patients' activation (PAM)
Measured with the Patient Activation Measure, for total group and for each condition separately. The questionnaire consists of 13 questions on a 5-point scale. The scores range from 0 to 100. The higher the score, the more capable a person is in self-management.
Medical Consumption within Health Care
Measured with the Medical Consumption Questionnaire (MCQ), for total group and for each condition separately. The questionnaire includes 16 questions related to frequently occurring contacts with health care providers. The items will be valued using standard cost prices in the Netherlands. The costs of medical consumption are calculated by multiplying the volumes of care by the cost per unit of care. This will be used for a cost-effectiveness analysis.
Productivity losses
Measured with the Productivity Costs Questionnaire (PCQ), for total group and for each condition separately. The questionnaire includes 9 questions related to the impact of disease on the ability of a person to perform work. The items will be valued using standard cost prices in the Netherlands. Productivity lossess are calculated by multiplying the volumes by cost prices per unit. This will be used for a cost-effectiveness analysis.
Full Information
NCT ID
NCT04127383
First Posted
October 10, 2019
Last Updated
March 14, 2023
Sponsor
Maastricht University
Collaborators
Netherlands Instititute for Health Services Research, TNO, University of Twente
1. Study Identification
Unique Protocol Identification Number
NCT04127383
Brief Title
Effectiveness and Implementation of the Assessment of Burden of Chronic Conditions (ABCC)-Tool
Official Title
Effectiveness, Cost-effectiveness and Implementation of the Assessment of Burden of Chronic Conditions (ABCC)-Tool in Patients With COPD, Asthma, Diabetes Mellitus Type 2 and Heart Failure: a Pragmatic Clustered Quasi-experimental Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
November 1, 2019 (Actual)
Primary Completion Date
November 1, 2022 (Actual)
Study Completion Date
November 1, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Maastricht University
Collaborators
Netherlands Instititute for Health Services Research, TNO, University of Twente
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is designed to evaluate the effectiveness and implementation of the Assessment of Burden of Chronic Conditions (ABCC)-tool for patients with COPD, asthma, diabetes mellitus type 2 or heart failure (and any combination of these conditions) in real-life routine practice. The ABCC-tool consists of a questionnaire, a visualisation using balloons that is based on cut-off points, and treatment advice. The ABCC-tool is intended to be used in daily healthcare practice, is designed to monitor a patient's integrated health status over time, to facilitate shared decision making, and to stimulate self-management. The study has a pragmatic clustered quasi-experimental design with two arms. The intervention group will use the ABCC-tool and the control group will receive usual care. The study will be implemented at a general practice-level, and has a follow-up period of 18 months. The primary outcome is change in perceived quality of care, as measured with the Patient Assessment of Chronic Illness Care (PACIC), as compared to usual care after 18 months. It is hypothesized that the change in perceived quality of care is significantly higher in the group using the ABCC-tool as compared to the group that receives usual care. Additionally the implementation of the ABCC-tool in general practices will be evaluated in 12 general practices. The implementation study will evaluate the context of caregivers with the Consolidated Framework for Implementation Research, the process of implementation with the RE-AIM framework, and fidelity to the intervention with the fidelity framework.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease, Asthma, Diabetes Mellitus, Type 2, Heart Failure
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Pragmatic clustered quasi-experimental study
Masking
Outcomes Assessor
Masking Description
Blinding of healthcare providers and patients is not possible due to the nature of the intervention, but the study team will be blind to treatment arms in the data set during data cleaning, handling of missing data, statistical analyses and drawing of conclusions.
Allocation
Non-Randomized
Enrollment
237 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ABCC-tool
Arm Type
Experimental
Arm Description
The intervention group will use the ABCC-tool during consultation with their healthcare provider. Healthcare providers in the intervention group will receive a short instructional film about the ABCC-tool before the start of the study. Additionally, healthcare providers from 12 practices will be invited for interviews, evaluating the context and process of implementation.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
The control group will receive usual care, and healthcare providers will not be instructed
Intervention Type
Device
Intervention Name(s)
Assessment of Burden of Chronic Conditions (ABCC)-tool
Intervention Description
The tool consists of a questionnaire, a visualisation using balloons, and treatment advice. A patient completes the questionnaire before consultation. The questionnaire measures the experienced burden of the chronic condition(s), and several risk factors. The questionnaire consists of a generic part and disease-specific parts. The generic questionnaire will be combined with any amount of disease-specific questionnaires (i.e. COPD, asthma, diabetes type 2 and heart failure), to form a single personalised scale and balloon chart for each individual patient. Outcomes of the questionnaire are visualised using balloons. The healthcare provider opens the visualisation during consultation. A balloon represents a domain, and the colour and height indicate a score on that domain. If a patient and healthcare provider select a balloon by clicking on it, treatment advice is shown by means of pop-ups. Based on the discussion following treatment advice, personal care plans can be determined.
Primary Outcome Measure Information:
Title
Perceived quality of care (PACIC): Patient Assessment of Chronic Illness Care
Description
Measured with the Patient Assessment of Chronic Illness Care, for total group. The scale has 20 items. Answers range from 1 to 5. Average scores (range 1-5) will be calculated. Higher scores mean more frequent presence of the aspect of structured chronic care.
Time Frame
0 months (baseline), 18 months
Secondary Outcome Measure Information:
Title
Perceived quality of care (PACIC): Patient Assessment of Chronic Illness Care
Description
Measured with the Patient Assessment of Chronic Illness Care, for total group and for each condition separately. The scale has 20 items. Answers range from 1 to 5. Average scores (range 1-5) will be calculated. Higher scores mean more frequent presence of the aspect of structured chronic care.
Time Frame
0 months (baseline), 6 months, 12 months
Title
Perceived quality of care (PACIC): Patient Assessment of Chronic Illness Care
Description
Measured with the Patient Assessment of Chronic Illness Care, for each condition separately. The scale has 20 items. Answers range from 1 to 5. Average scores (range 1-5) will be calculated. Higher scores mean more frequent presence of the aspect of structured chronic care.
Time Frame
0 months (baseline), 18 months
Title
Quality of life (EQ-5D-5L)
Description
Measured with the EuroQol-5D-5L, for total group and for each condition separately. The scale consists of the EQ-5D-5L descriptive system with 5 questions, and a VAS-scale. Answers range from 1 (best) to 5 (worst). EQ-5D-5L health states, defined by the EQ-5D-5L descriptive system, will be converted into a single index value (Dutch values). The EQ-5D-5L VAS will also be determined.
Time Frame
0 months (baseline), 6 months, 12 months, 18 months
Title
Capability well-being (ICECAP-A)
Description
Measured with the ICEpop CAPability measure for Adults, for total group and for each condition separately. The questionnaire consists of 5 questions. Answers range from 1 (no capability) to 4 (full capability for an attribute). A tariff value for an overall state can be calculated by summing the values across the individual attributes. This code will allow calculation of ICECAP-A tariffs for each respondent in a study
Time Frame
0 months (baseline), 6 months, 12 months, 18 months
Title
Patients' activation (PAM)
Description
Measured with the Patient Activation Measure, for total group and for each condition separately. The questionnaire consists of 13 questions on a 5-point scale. The scores range from 0 to 100. The higher the score, the more capable a person is in self-management.
Time Frame
0 months (baseline), 6 months, 12 months, 18 months
Title
Medical Consumption within Health Care
Description
Measured with the Medical Consumption Questionnaire (MCQ), for total group and for each condition separately. The questionnaire includes 16 questions related to frequently occurring contacts with health care providers. The items will be valued using standard cost prices in the Netherlands. The costs of medical consumption are calculated by multiplying the volumes of care by the cost per unit of care. This will be used for a cost-effectiveness analysis.
Time Frame
0 (baseline), 3, 6, 9, 12, 15 and 18 months
Title
Productivity losses
Description
Measured with the Productivity Costs Questionnaire (PCQ), for total group and for each condition separately. The questionnaire includes 9 questions related to the impact of disease on the ability of a person to perform work. The items will be valued using standard cost prices in the Netherlands. Productivity lossess are calculated by multiplying the volumes by cost prices per unit. This will be used for a cost-effectiveness analysis.
Time Frame
0 (baseline), 3, 6, 9, 12, 15 and 18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
diagnosis COPD, asthma, Diabetes Mellitus type 2 and/or heart failure
can understand and read the Dutch language
Exclusion Criteria:
COPD or asthma: used prednisone due to an exacerbation less than six weeks ago
Heart failure or diabetes mellitus type 2: hospitalized less than six weeks ago
Healthcare providers or patients who have already used the Assessment of Burden of COPD-tool are excluded from the control group
Patients who have already used the Assessment of Burden of COPD-tool will be excluded from the intervention group
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Onno CP van Schayck, Prof.
Organizational Affiliation
Maastricht University
Official's Role
Study Director
Facility Information:
Facility Name
Maastricht University
City
Maastricht
State/Province
Limburg
ZIP/Postal Code
6200MD
Country
Netherlands
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Deidentified individual data can be shared with researchers who provide a methodologically sound proposal.
Citations:
PubMed Identifier
33203626
Citation
Boudewijns EA, Claessens D, Joore M, Keijsers LCEM, van Schayck OCP, Winkens B, Gidding-Slok AHM. Effectiveness and cost-effectiveness of the Assessment of Burden of Chronic Conditions (ABCC) tool in patients with COPD, asthma, diabetes mellitus type 2 and heart failure: protocol for a pragmatic clustered quasi-experimental study. BMJ Open. 2020 Nov 17;10(11):e037693. doi: 10.1136/bmjopen-2020-037693.
Results Reference
derived
Links:
URL
https://software.memic.maastrichtuniversity.nl/ziektelastmeter/
Description
Related Info
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Effectiveness and Implementation of the Assessment of Burden of Chronic Conditions (ABCC)-Tool
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