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Dietary Advice on Prescription in Kungsbacka (DAP_K)

Primary Purpose

Overweight

Status
Unknown status
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Lifestyle counseling
Sponsored by
Halmstad University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overweight focused on measuring Overweight, Obesity, lifestyle counseling

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • BMI 28-35

Exclusion Criteria:

  • Severe disease

Sites / Locations

  • Carema husläkarnaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Lifestyle counseling

Control group

Arm Description

Lifestyle counseling

Control group

Outcomes

Primary Outcome Measures

BMI
Lifestyle intervention

Secondary Outcome Measures

LDL cholesterol
Lifestyle intervention

Full Information

First Posted
June 29, 2011
Last Updated
July 1, 2011
Sponsor
Halmstad University
Collaborators
Carema, Region Halland
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1. Study Identification

Unique Protocol Identification Number
NCT01385930
Brief Title
Dietary Advice on Prescription in Kungsbacka
Acronym
DAP_K
Official Title
A New Concept for Lifestyle Change, Dietary Advice on Prescription (DAP) in Combination With Motivational Interviewing (MI), Social Support and Mobile Services
Study Type
Interventional

2. Study Status

Record Verification Date
March 2011
Overall Recruitment Status
Unknown status
Study Start Date
March 2011 (undefined)
Primary Completion Date
December 2014 (Anticipated)
Study Completion Date
December 2015 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Halmstad University
Collaborators
Carema, Region Halland

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the study is to evaluate self-reported adherence to and the effects of an intervention model consisting of individualized prescribed dietary advice (DAP) in combination with Motivational Interviewing (MI), social support and mobile services in obese patients in primary health care. The specific aim is to relate effects of the intervention model to self-reported health, biomarkers for coronary heart disease, diabetes, some cancer forms, sleep duration and quality, health economy, oral health, dietary intake and physical activity. This is a two-armed randomized controlled study. The arms are: 1) Control group (care as usual) and 2) Experimental group (MoR). The volunteers will be consecutively, for each sex, randomized to the experimental and the control group, respectively. The experimental group will receive DAP together with Motivational interviewing up to six months after the start of the study. From six months up to 24 months the participants will receive social support online and mobile services. The control group will receive dietary information according to the "Habo model". The previously mentioned diet will be recommended to both the control group and the experimental group since it is the method in which the investigators give the information they want to study and not the diet per se. Thus, it is only the way the investigators give dietary information that differs between the groups. The study also includes qualitative interviews. The aim of these studies is to gain understanding of patients' and health professionals' experience and attitudes around food, lifestyle and support functions associated with dietary change. The sampling approach involves the purposeful selection of cases with a wide range of variation, which means that the researcher selects people who are able to provide rich information about the current issue. To achieve diversity, it is useful that both women and men are involved in the studies, as well as people of different ages and with different experiences of providing or receiving dietary advice. About 15-20 people will participate in each interview study.
Detailed Description
The investigators assume a difference in BMI (body mass index; kg/m x m) of 2 units, a standard deviation of 4.5 units, a power of 80 %, an alfa error of 5 % I a two-tailed test, the investigators would need at least 80 individuals in the experimental group and in the control group, respectively. With 80 individuals in each group and the assumption of 5 % adherence (4 individuals) in the control group, the investigators would be able to detect an adherence of 21 % or higher (at least 17 individuals) in the experimental group with 80 % power. The alfa error is set to 5 % in a two-tailed test with the null hypothesis that the adherence is the same in both groups. Therefore the investigators plan a study with at least 100 individuals in each group and assume that 20 % will not complete the study. The evaluation of the quantitative studies will be performed in three ways: 1) Process evaluation, that will focus on intermediate outcomes such as knowledge, attitudes, motivation and readiness for change. 2) Effect evaluation will be used to evaluate the effect of the intervention programme on the subjects' behavior such as dietary intake and physical activity level. 3) Outcome evaluation will measure the total effect of the intervention programme, in this case variables that measures indicators for health and disease, such as SF-36, EQ-5D, SHIS, serum cholesterol, blood pressure, BMI, waist circumference etc. Intention-to-treat (ITT) analysis will be used to assess effects on outcome measures. Variables not normally distributed will be logarithmically transformed. Paired t-test will be used to assess change within groups and unpaired t-tests to compare mean changes between groups. Non-parametric statistics, Wilcoxon Signed Ranks Test and Mann-Whitney U-Test will be used for ordinal data such as questionnaires. Two-tailed tests will be used and a p-value less than 0.05 will be considered statistically significant. Qualitative data will be analyzed by content analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight
Keywords
Overweight, Obesity, lifestyle counseling

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Lifestyle counseling
Arm Type
Experimental
Arm Description
Lifestyle counseling
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Control group
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle counseling
Intervention Description
Lifestyle counseling
Primary Outcome Measure Information:
Title
BMI
Description
Lifestyle intervention
Time Frame
two years
Secondary Outcome Measure Information:
Title
LDL cholesterol
Description
Lifestyle intervention
Time Frame
two years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: BMI 28-35 Exclusion Criteria: Severe disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marie Ewe, Nurse
Phone
0733-132999
Email
Marie.Brautigam-Ewe@lthalland.se
First Name & Middle Initial & Last Name or Official Title & Degree
Jörgen Månsson, MD
Phone
0705-776711
Email
Jorgen.Mansson@carema.se
Facility Information:
Facility Name
Carema husläkarna
City
Kungsbacka
State/Province
Halland
ZIP/Postal Code
434 30
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie Ewe, Nurse
Phone
0733-132999
Email
Marie.Brautigam-Ewe@lthalland.se
First Name & Middle Initial & Last Name & Degree
Jörgen Månsson, MD
Phone
0705-776711
Email
Jorgen.Mansson@carema.se
First Name & Middle Initial & Last Name & Degree
Gunnar Johansson, Ph.D.
First Name & Middle Initial & Last Name & Degree
Marie Ewe, Nurse

12. IPD Sharing Statement

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Dietary Advice on Prescription in Kungsbacka

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