N/A
N=23
SHARE-D: a Decision Tool to Help Patients Make Informed Lifestyle Choices
Health Behavior
Bottom Line
View on ClinicalTrials.gov: NCT03276546 ↗Enrolled (actual)
23
Serious AEs
0.0%
Results posted
Jan 2024
Primary outcome: Primary: Recruitment Rate — 45; 23 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- shared decision-making tool (SHARE-D) (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Queen's University, Belfast
- Primary completion
- Jan 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Recruitment Rate |
45; 23 | — |
| SECONDARY Completion Rate |
20 | — |
| SECONDARY Diet Behaviour - Fibre Intake |
35.35; 34.60 | — |
| SECONDARY Physical Activity Behaviour |
14; 16 | — |
| SECONDARY Objective Measure of Physical Activity |
16; 5; 10; 11 | — |
Summary
More information is needed about effective ways to help people begin to change their lifestyle behaviours, particularly physical activity and diet. The investigators propose to test a 'tool' that can be used to guide discussions between people and health professionals about their physical activity and diet habits, so that people may be supported better in making decisions about why and how they might begin to fit more exercise and healthy food into their daily routines and make long-term changes. The investigators will explore the feasibility of using this tool in general practice, reviewing behaviours after 1 and 3 months. Patients' and healthcare professionals' views of its use and how it influenced decisions will inform development of the tool's design and a study of its effectiveness in helping people to begin to change their behaviour and achieve healthy lifestyles.
Eligibility Criteria
Inclusion Criteria
- Aged 18 years or over
- With or at high risk of coronary heart disease
- Overweight or physically inactive
Exclusion Criteria
- Unable to complete questionnaires
- Unable to make independent changes to physical activity or diet habits
Data sourced from ClinicalTrials.gov (NCT03276546). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.