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Feasibility of a Preventive Program Against Lifestyle Related Diseases

Primary Purpose

Type-2 Diabetes, Cardiovascular Diseases, Chronic Obstructive Pulmonary Disease (COPD)

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Lifestyle intervention
Sponsored by
University of Southern Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Type-2 Diabetes focused on measuring Tailored lifestyle intervention, Selective prevention, Primary care, Web based health risk assessment, Patient-centered health information system, Lifestyle intervention, preventive treatment

Eligibility Criteria

30 Years - 59 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients listed to one of the participating GPs
  • Place of residence: One of the two participating municipalities in the Region of Southern Denmark.
  • Year of birth: 1957-1986

Exclusion Criteria:

  • None

Sites / Locations

  • Research Programme on Health Promotion and Prevention, National Institute of Public Health, University of Southern Denmark,
  • Research Unit of General Practice, Dept. of Public Health, University of Southern Denmark,
  • Center of Health Economics Research, Department of Business and Economics, University of Southern Denmark
  • Department of Sports Science and Clinical Biomechanics, Musculoskeletal Function and Physiotherapy, University of Southern Denmark
  • Research Group for Information Systems, Department of Informatics, University of Oslo
  • Center for Primary Health Care Research, Department of Clinical Sciences

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Lifestyle intervention

Arm Description

All included citizens receive a questionnaire to estimate risk of disease and risk behavior. Information about lifestyle is collated with existing Electronic Patient Record (EPR) data and the citizen's risk of lifestyle-related disease is estimated based on validated algorithms for risk of type-2 diabetes, cardiovascular disease and COPD (Stratification). All citizens receive an electronic health profile and targeted advice. Citizens at increased risk of disease are offered a preventive program at the GP including an initial health examination and subsequent lifestyle counselling. Citizens with risk behavior are offered lifestyle counselling in the municipality and community health services, if necessary. Citizens diagnosed with a lifestyle related disease are already being treated by the GP, and therefore, like citizens with a healthy lifestyle, they are not offered any further services.

Outcomes

Primary Outcome Measures

Change in proportion of citizens at increased risk of lifestyle related disease from baseline to the 12 weeks follow up
Questionnaire. Risk of lifestyle related disease is estimated based on the validated algorithms described under Detailed Study Description

Secondary Outcome Measures

Evaluation of the patient centered health information system with focus on design, usability and effect of the decision support system.
Focus group interviews within three months before study start. The focus groups comprise 6 GPs and 2 practice staff members, 9 municipality staff members, 9 citizens and representatives from 6 stakeholder organizations, respectively. Observational studies focusing on 6-8 citizens during the 12 weeks study period with focus on all situations where the health information system is used (at home, at the GPs, etc.). Questionnaire to all participating citizens within 1 month following the 12 weeks study period and to all participating GPs and municipality staff members following each study related patient encounter.
Process evaluation focusing on the intervention in general practice.
Observational studies during 10-15 behavior counseling sessions in different general practices, followed by qualitative interviews with the participating citizens, GPs and practice staff. Questionnaire to all participating GPs and practice staff members following each study related patient encounter.
Quality of Life Subscale on the Hip injury and Osteoarthritis Outcome Score (HOOS)/Knee Injury and Osteoarthritis Outcome Score (KOOS)
Participants replying "yes" to any of the osteoarthritis related questions on hip/knee pain, GP care seeking or surgery at baseline will receive additional questions on knee/hip related quality of life.
Patient enablement following the behavior counselling session at the GP.
Questionnaire incl. Patient Enablement Instrument (PEI)
Patient reported self-efficacy
Questionnaire incl. The General Self-Efficacy Scale
Patient reported mental well-being.
Questionnaire incl. The short Warwick-Edinburgh Mental Well-being Scale (SWEMWBS)
Process evaluation focusing on the common training course for enrolled GPs, practice staff and health professionals from the municipalities.
Observational studies during the common training course and questionnaire at the end of the course.
GPs and the citizens preferences with regard to the content of the behavior counselling session, and change in preferences from baseline to the 12 weeks follow up.
Questionnaire using discrete choice modelling.
Patients' perceptions of relational empathy following the behavior counselling session at the GP.
Questionnaire including The Consultation And Relational Empathy (CARE) measure.
Patient reported Meaning-Making and Health
Questionnaire with items sampled from the validated questionnaire SoMe (Sources of Meaning)
Patient reported Spiritual Wellbeing
Questionnaire including the validated FACITSp scale
Patient reported Religious belief and practices
Questionnaire with items sampled from the validated questionnaire European Value Study (EVS)
GP reported perceived importance of communication on existential and spiritual issues
Questionnaire with two tested items developed for this study
GP reported Self-efficacy and barriers in communication on existential and spiritual issues
Questionnaire with items sampled from the validated Self-efficacy questionnaire
GP reported Personal belief
Questionnaire with items sampled from the validated questionnaire European Value Study (EVS)

Full Information

First Posted
April 29, 2016
Last Updated
April 26, 2019
Sponsor
University of Southern Denmark
Collaborators
University of Oslo, Lund University
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1. Study Identification

Unique Protocol Identification Number
NCT02797392
Brief Title
Feasibility of a Preventive Program Against Lifestyle Related Diseases
Official Title
Early Detection and Prevention of Lifestyle Related Diseases - a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
September 2016 (Actual)
Primary Completion Date
February 28, 2017 (Actual)
Study Completion Date
December 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern Denmark
Collaborators
University of Oslo, Lund University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The continuously increasing prevalence of cardiovascular diseases, type-2 diabetes, and COPD is a major health problem in developed countries and is mainly caused by an unhealthy lifestyle. Most important lifestyle related causes of morbidity and mortality are smoking, obesity and physical inactivity, and increasing rates of obesity and physical inactivity in combination with smoking will lead to an increase in the number of patients with lifestyle related diseases in the coming decades. There is, therefore, an urgent need to identify and establish strategies and to implement interventions, allowing for the identification and management of citizens at increased risk of disease. Two recent systematic reviews of general practice based health checks suggest that people at increased risk of a chronic disease may benefit from a targeted approach to health checks. Targeted or selective preventive actions are a generally accepted and well integrated part of the health care system (e.g. treatment of hypertension and hyperlipidemia). However, selective prevention is challenged in terms of how to identify citizens at increased risk of disease in the general population in order to start the indicated preventive actions. The aim of the present pilot study is to test the acceptability, feasibility and short-term effect of a selective preventive program that systematically helps citizens evaluate individual risk of lifestyle related disease and offers targeted and coordinated preventive services in the primary health care sector. The intervention comprises four elements: 1) Systematic collection of information on lifestyle risk factors using questionnaire 2) Risk estimation and stratification into risk groups based on questionnaire data and information from the electronic patient record (EPR) using validated risk estimation models, 3) An individual electronic health profile with personalized advise on lifestyle change and 4) targeted preventive services at the general practitioner (GP) or the municipality for citizens at risk of lifestyle disease and citizens with risk behavior, respectively. The intervention is supported by a patient-centered health information system that facilitates informed patient action and integrates general practice and municipality health care providers.
Detailed Description
Recruitment strategy: The study is carried out in two municipalities in the Region of Southern Denmark (Haderslev and Varde municipality. Total number of inhabitants: 98.925). All general practitioners in the two municipalities (n=68) have been invited, and a total of 47 have agreed to participate in the study. A total of 200 citizens born 1957-1986 are selected from the patient list of each participating GP. Before selection, the citizens are stratified into households, and subsequently households are randomly selected until the total number of citizens per enrolled GP reaches 200. In selection of households the proportion of citizens living alone and the proportion of citizens living with one or more potential participants is taken into account. No disease-related criteria for excluding a citizen are defined prior to the study. The selected citizens are invited to participate and asked to sign a declaration of consent. Risk stratification and preventive services offered: Enrolled participants receive a 15-item questionnaire on lifestyle, familiar disposition of lifestyle disease and selected symptoms. From the individual electronic patient records (EPR) at the GP information on diagnoses and treatment of COPD, type-2 diabetes, hyperlipidemia, hypertension and ischemic heart disease are drawn. Based on questionnaire and EPR data the participants are stratified into four groups: 1) Citizens with an already diagnosed lifestyle related disease, 2) Citizens with an increased risk of lifestyle related disease, 3) Citizens with risk behavior and 4) Citizens with a healthy lifestyle. Citizens in group 1 are already being treated and/or receive behavioral interventions and are therefore not the primary target of this study. Citizens in group 2 has a calculated increased risk of lifestyle related disease(s) based on validated predictive models for risk of COPD, type-2 diabetes and cardiovascular disease. The risk of COPD is calculated using the COPD-PS screener algorithm taking into account information on age, total cigarette consumption and respiratory symptoms. The risk of type-2 diabetes is calculated based on the algorithm used in the Addition study including information on age, gender, BMI, history of hypertension, physical activity and family history of diabetes. The cut-off value for being at risk of type-2 diabetes, and COPD follows the recommendations of the two models. The risk of cardiovascular disease is calculated using the Heart Score BMI score based on information about age, gender, smoking status and BMI. An increased risk of cardiovascular disease is defined in citizens with a β‰₯5% risk of dying of cardiovascular disease within the next 10 years. Citizens in group 2 are offered a preventive program at the GP including an initial health examination and subsequent behavior counselling. Citizens in group 3 are defined by having a BMI>35, being daily smoker, having a high risk alcohol consumption, having unhealthy eating habits and/or low physical activity. Evaluation of eating habits is based on the recommendations in the Swedish National Guidelines on Disease Prevention, and evaluation of alcohol consumption and physical activity is based on recommendations from the Danish Health Authority. Citizens in group 3 are offered behavior counselling in the municipality and community health services, if necessary. Citizens in group 4 are not offered any further services. Electronic health information system: The intervention is supported by a patient-centered health information system that facilitates informed patient action based on the predictive model for identification and stratification of citizens to the appropriate care providers and that supports the initiation and follow up of preventive care through the provision of health information resources, decision aids, risk calculators, personalized motivational messages and integrates primary care and municipality health care providers. Common training course: Before the study commences enrolled GPs, practice staff and health professionals from the municipalities are offered a common training course. The aim of the course is to train the specific intervention elements and to improve the inter-sectoral knowledge and collaboration on prevention of lifestyle diseases. Evaluation: Evaluation of the study will be carried out using quantitative as well as qualitative research methods. Details on evaluation methods are included in section 9. Results of the present pilot study will be used for the adjustment of the intervention prior to a large scale study comprising 10 municipalities, up to 360 GPs and 200.000 citizens.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type-2 Diabetes, Cardiovascular Diseases, Chronic Obstructive Pulmonary Disease (COPD)
Keywords
Tailored lifestyle intervention, Selective prevention, Primary care, Web based health risk assessment, Patient-centered health information system, Lifestyle intervention, preventive treatment

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9400 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lifestyle intervention
Arm Type
Experimental
Arm Description
All included citizens receive a questionnaire to estimate risk of disease and risk behavior. Information about lifestyle is collated with existing Electronic Patient Record (EPR) data and the citizen's risk of lifestyle-related disease is estimated based on validated algorithms for risk of type-2 diabetes, cardiovascular disease and COPD (Stratification). All citizens receive an electronic health profile and targeted advice. Citizens at increased risk of disease are offered a preventive program at the GP including an initial health examination and subsequent lifestyle counselling. Citizens with risk behavior are offered lifestyle counselling in the municipality and community health services, if necessary. Citizens diagnosed with a lifestyle related disease are already being treated by the GP, and therefore, like citizens with a healthy lifestyle, they are not offered any further services.
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle intervention
Intervention Description
1) Systematic collection of information on lifestyle risk factors using questionnaire 2) Risk estimation and stratification into risk groups based on questionnaire data and information from the electronic patient record (EPR) using validated risk estimation models, 3) An individual electronic health profile with personalized advise on lifestyle change and 4) targeted preventive services incl. lifestyle counseling at the GP or the municipality for citizens at increased risk of lifestyle disease and citizens with risk behavior, respectively.
Primary Outcome Measure Information:
Title
Change in proportion of citizens at increased risk of lifestyle related disease from baseline to the 12 weeks follow up
Description
Questionnaire. Risk of lifestyle related disease is estimated based on the validated algorithms described under Detailed Study Description
Time Frame
At baseline and within 1 month following the 12 weeks study period.
Secondary Outcome Measure Information:
Title
Evaluation of the patient centered health information system with focus on design, usability and effect of the decision support system.
Description
Focus group interviews within three months before study start. The focus groups comprise 6 GPs and 2 practice staff members, 9 municipality staff members, 9 citizens and representatives from 6 stakeholder organizations, respectively. Observational studies focusing on 6-8 citizens during the 12 weeks study period with focus on all situations where the health information system is used (at home, at the GPs, etc.). Questionnaire to all participating citizens within 1 month following the 12 weeks study period and to all participating GPs and municipality staff members following each study related patient encounter.
Time Frame
Three months before the study period, ongoing during the 12 weeks study period and within one month following the 12 weeks study period, respectively.
Title
Process evaluation focusing on the intervention in general practice.
Description
Observational studies during 10-15 behavior counseling sessions in different general practices, followed by qualitative interviews with the participating citizens, GPs and practice staff. Questionnaire to all participating GPs and practice staff members following each study related patient encounter.
Time Frame
Ongoing during the 12 weeks study period
Title
Quality of Life Subscale on the Hip injury and Osteoarthritis Outcome Score (HOOS)/Knee Injury and Osteoarthritis Outcome Score (KOOS)
Description
Participants replying "yes" to any of the osteoarthritis related questions on hip/knee pain, GP care seeking or surgery at baseline will receive additional questions on knee/hip related quality of life.
Time Frame
At baseline
Title
Patient enablement following the behavior counselling session at the GP.
Description
Questionnaire incl. Patient Enablement Instrument (PEI)
Time Frame
Within one week following each behavior counselling session at the GP.
Title
Patient reported self-efficacy
Description
Questionnaire incl. The General Self-Efficacy Scale
Time Frame
At baseline
Title
Patient reported mental well-being.
Description
Questionnaire incl. The short Warwick-Edinburgh Mental Well-being Scale (SWEMWBS)
Time Frame
At baseline and within 1 month following the 12 weeks study period.
Title
Process evaluation focusing on the common training course for enrolled GPs, practice staff and health professionals from the municipalities.
Description
Observational studies during the common training course and questionnaire at the end of the course.
Time Frame
The common training course before study start.
Title
GPs and the citizens preferences with regard to the content of the behavior counselling session, and change in preferences from baseline to the 12 weeks follow up.
Description
Questionnaire using discrete choice modelling.
Time Frame
At baseline and within 1 month following the 12 weeks study period.
Title
Patients' perceptions of relational empathy following the behavior counselling session at the GP.
Description
Questionnaire including The Consultation And Relational Empathy (CARE) measure.
Time Frame
Within one week following each behavior counselling session at the GP.
Title
Patient reported Meaning-Making and Health
Description
Questionnaire with items sampled from the validated questionnaire SoMe (Sources of Meaning)
Time Frame
Within 1 month following the 12 weeks study period.
Title
Patient reported Spiritual Wellbeing
Description
Questionnaire including the validated FACITSp scale
Time Frame
Within 1 month following the 12 weeks study period.
Title
Patient reported Religious belief and practices
Description
Questionnaire with items sampled from the validated questionnaire European Value Study (EVS)
Time Frame
Within 1 month following the 12 weeks study period
Title
GP reported perceived importance of communication on existential and spiritual issues
Description
Questionnaire with two tested items developed for this study
Time Frame
Within 1 month following the 12 weeks study period.
Title
GP reported Self-efficacy and barriers in communication on existential and spiritual issues
Description
Questionnaire with items sampled from the validated Self-efficacy questionnaire
Time Frame
Within 1 month following the 12 weeks study period.
Title
GP reported Personal belief
Description
Questionnaire with items sampled from the validated questionnaire European Value Study (EVS)
Time Frame
Within 1 month following the 12 weeks study period.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients listed to one of the participating GPs Place of residence: One of the two participating municipalities in the Region of Southern Denmark. Year of birth: 1957-1986 Exclusion Criteria: None
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jens SΓΈndergaard
Organizational Affiliation
Research Unit of General Practice, Dept. of Public Health, University of Southern Denmark, DK-5000 Odense C, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Research Programme on Health Promotion and Prevention, National Institute of Public Health, University of Southern Denmark,
City
Copenhagen
ZIP/Postal Code
DK-1353
Country
Denmark
Facility Name
Research Unit of General Practice, Dept. of Public Health, University of Southern Denmark,
City
Odense C
ZIP/Postal Code
DK-5000
Country
Denmark
Facility Name
Center of Health Economics Research, Department of Business and Economics, University of Southern Denmark
City
Odense
ZIP/Postal Code
DK-5230
Country
Denmark
Facility Name
Department of Sports Science and Clinical Biomechanics, Musculoskeletal Function and Physiotherapy, University of Southern Denmark
City
Odense
ZIP/Postal Code
DK-5230
Country
Denmark
Facility Name
Research Group for Information Systems, Department of Informatics, University of Oslo
City
Oslo
ZIP/Postal Code
0373
Country
Norway
Facility Name
Center for Primary Health Care Research, Department of Clinical Sciences
City
MalmΓΈ
ZIP/Postal Code
SE-205 02
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No
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Feasibility of a Preventive Program Against Lifestyle Related Diseases

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