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The RISAP-study: a Complex Intervention in Risk Communication and Shared Decision-making in General Practice (RISAP)

Primary Purpose

High Cholesterol, Cardiovascular Disease

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Training programme
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for High Cholesterol focused on measuring Shared decision-making, Risk information, Decision aids

Eligibility Criteria

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

Inclusion Criteria:

- GPs in Region Central and Region North, Denmark, are invited to the study.

Patients are at least 18 years old, and have high cholesterol corresponding to a recommendation for cholesterol-reducing medication according to Danish clinical guideline for general practice. The patients are recruited after their high cholesterol has been detected and when treatment options are to be discussed.

Exclusion Criteria:

- Patients with CVD or DM are excluded from the study, as are patients already receiving cholesterol-reducing medication and patients unable to speak and read Danish.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Training, decision making

    Training, usual practice

    Arm Description

    General practitioners receive training in shared decision-making and risk communication, and use their newly acquired skills in real-life consultations with 7 patients with high cholesterol.

    The control group GPs will receive 2 hours of training in the primary care guideline for prevention of cardiovascular disease

    Outcomes

    Primary Outcome Measures

    The primary patient outcome is adherence to treatment choice.

    Secondary Outcome Measures

    satisfaction with decision.
    self-rated health
    anxiety
    enablement
    satisfaction with communication,
    satisfaction and confidence in decision
    number of contacts to health services

    Full Information

    First Posted
    August 20, 2010
    Last Updated
    May 8, 2017
    Sponsor
    University of Aarhus
    Collaborators
    TrygFonden, Denmark
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01187056
    Brief Title
    The RISAP-study: a Complex Intervention in Risk Communication and Shared Decision-making in General Practice
    Acronym
    RISAP
    Official Title
    The RISAP-study: a Complex Intervention in Risk Communication and Shared Decision-making in General Practice
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2012
    Overall Recruitment Status
    Completed
    Study Start Date
    November 2007 (undefined)
    Primary Completion Date
    July 2012 (Actual)
    Study Completion Date
    July 2012 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Aarhus
    Collaborators
    TrygFonden, Denmark

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    General practitioners (GPs) and patients find it difficult to talk about risk of future disease, especially when patients have asymptomatic conditions, and treatment options are unlikely to cause immediate perceptible improvements in well-being. Further studies in risk communication for disease prevention are needed, as are studies about risk communication training for GPs. Aim: 1) to systematically develop, describe and evaluate a complex intervention comprising a training programme for GPs in risk communication and shared decision-making, 2) to evaluate the effect of the training programme on real-life consultations between GPs and patients with high cholesterol levels, and 3) to evaluate patients' reactions during and after the consultations. Hypothesis: 1) patients have better adherence to chosen treatment. The effect of the complex intervention, based around a training programme, will be evaluated in a cluster-randomised controlled trial with an intervention group and an active control group with 40 GPs and 280 patients in each group. The GPs receive a questionnaire at baseline and after 6 months about their attitudes towards risk communication and cholesterol-reducing medication. After each consultation with a participating high cholesterol-patient, the GPs will complete a questionnaire about decision satisfaction. The patients will receive a questionnaire at baseline and after 3 and 6 months. It includes questions about adherence to chosen treatment, self-rated health, patient enablement, and risk communication and decision-making effectiveness. Prescriptions, contacts to the health services, and cholesterol level will be drawn from the register of the National Health Service of Denmark at baseline and at 6 months. In both intervention group and active control group, 12 consultations will be observed and tape-recorded. The consultations will be divided between 4 GPs with each 3 patients. The patients from these 24 consultations will be interviewed immediately after the consultation and re-interviewed after 6 months.Eight purposefully selected GPs from the intervention group will be interviewed in a focus group 6 months after participation in the training programme. The process and context of the RISAP-study will be investigated in detail using an action research approach, in order to describe and analyse research choices, adaptation of intervention model to the specific context, and GPs' and patients' reactions to trial participation.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    High Cholesterol, Cardiovascular Disease
    Keywords
    Shared decision-making, Risk information, Decision aids

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    179 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Training, decision making
    Arm Type
    Experimental
    Arm Description
    General practitioners receive training in shared decision-making and risk communication, and use their newly acquired skills in real-life consultations with 7 patients with high cholesterol.
    Arm Title
    Training, usual practice
    Arm Type
    Active Comparator
    Arm Description
    The control group GPs will receive 2 hours of training in the primary care guideline for prevention of cardiovascular disease
    Intervention Type
    Behavioral
    Intervention Name(s)
    Training programme
    Other Intervention Name(s)
    decision making, decision aids
    Intervention Description
    2 x 2 hours of training (workshops)
    Primary Outcome Measure Information:
    Title
    The primary patient outcome is adherence to treatment choice.
    Time Frame
    2010-08-01 - 2011-04-01
    Secondary Outcome Measure Information:
    Title
    satisfaction with decision.
    Time Frame
    2010-08-01 - 2011-04-01
    Title
    self-rated health
    Time Frame
    2010-08-01 - 2011-04-01
    Title
    anxiety
    Time Frame
    2010-08-01 - 2011-04-01
    Title
    enablement
    Time Frame
    2010-08-01 - 2011-04-01
    Title
    satisfaction with communication,
    Time Frame
    2010-08-01 - 2011-04-01
    Title
    satisfaction and confidence in decision
    Time Frame
    2010-08-01 - 2011-04-01
    Title
    number of contacts to health services
    Time Frame
    2010-08-01 - 2011-04-01

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: - GPs in Region Central and Region North, Denmark, are invited to the study. Patients are at least 18 years old, and have high cholesterol corresponding to a recommendation for cholesterol-reducing medication according to Danish clinical guideline for general practice. The patients are recruited after their high cholesterol has been detected and when treatment options are to be discussed. Exclusion Criteria: - Patients with CVD or DM are excluded from the study, as are patients already receiving cholesterol-reducing medication and patients unable to speak and read Danish.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Janus L Thomsen, MD, PhD
    Organizational Affiliation
    University of Aarhus
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    24040920
    Citation
    Kirkegaard P, Edwards A, Risor MB, Thomsen JL. Risk of cardiovascular disease? A qualitative study of risk interpretation among patients with high cholesterol. BMC Fam Pract. 2013 Sep 16;14:137. doi: 10.1186/1471-2296-14-137.
    Results Reference
    derived
    PubMed Identifier
    23113909
    Citation
    Kirkegaard P, Risor MB, Edwards A, Junge AG, Thomsen JL. Speaking of risk, managing uncertainty: decision-making about cholesterol-reducing treatment in general practice. Qual Prim Care. 2012;20(4):245-52.
    Results Reference
    derived
    PubMed Identifier
    20860820
    Citation
    Kirkegaard P, Edwards AG, Hansen B, Hansen MD, Jensen MS, Lauritzen T, Risoer MB, Thomsen JL. The RISAP-study: a complex intervention in risk communication and shared decision-making in general practice. BMC Fam Pract. 2010 Sep 22;11:70. doi: 10.1186/1471-2296-11-70.
    Results Reference
    derived

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    The RISAP-study: a Complex Intervention in Risk Communication and Shared Decision-making in General Practice

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