Objective: Aim of the present study is to test the effectiveness of a preventive intervention that helps to maintain healthy diet during difficult situations by means of coping plans (plans how to deal with situations that might threaten adherence…
ID
Source
Brief title
Condition
- Other condition
Synonym
Health condition
overgewicht
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Outcome measures: 1) adherence to healthy diet (electronic diet diary qualified
by a biomarker) and weight loss, 2) coping plans, coping self-efficacy, and
awareness of threats to adherence.
Secondary outcome
not applicable
Background summary
Research questions: 1) Examine the effectiveness of the intervention in terms
of adherence to healthy diet and weight loss (primary outcomes); 2) Examine the
effectiveness of the intervention in terms of coping plans, better coping
self-efficacy, and awareness of potential threats for maintaining healthy diet
(secondary outcomes); 3) Examine to what extent the effectiveness of the
intervention is moderated by variables relating to self-regulatory competence.
Intervention: A minimal intervention aimed at improving self-management of
health behavior that has proven effective in previous research will be tailored
to address the topic of maintaining attempts to reduce overweight. Power
analysis: With a power of .90 and alpha set at .05, a minimum of 90 patients
per condition allows for the detection of medium effects on the primary outcome
variable. Time schedule: Year 1: Development and pilot of intervention,
recruitment of patients; Year 2: Start of intervention, baseline
data-collection; Year 3: Continued intervention and follow-up data-collection;
Year 4: data-analyses, preparation of manuscripts.
Study objective
Objective: Aim of the present study is to test the effectiveness of a
preventive intervention that helps to maintain healthy diet during difficult
situations by means of coping plans (plans how to deal with situations that
might threaten adherence to healthy diet) in overweight people who are at risk
for diabetes and motivated to reduce weight.
Study design
Study design: A prospective randomized controlled design with a 12-month
follow-up will be employed.
Study burden and risks
not applicable
Postbus 80140
3508 TC Utrecht
NL
Postbus 80140
3508 TC Utrecht
NL
Listed location countries
Age
Inclusion criteria
BMI>28 (moderate overweight and obese); motivation for weight loss
Exclusion criteria
BMI>40 (morbid obese); insuffient mastery of Dutch in speech and writing; currently involved in treatment for overweight.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL20539.041.07 |