Technology Assisted Dietary Assessment and Advice (TADAA) Feasibility Study
Not Applicable
- Conditions
- Cardiovascular diseaseCardiovascular - Coronary heart diseaseDiet and Nutrition - Other diet and nutrition disorders
- Registration Number
- ACTRN12623001084673
- Lead Sponsor
- Edith Cowan University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Participants will be included if they are adults scheduled for elective cardiac surgery with a wait time greater than 4 weeks
Exclusion Criteria
Participants excluded if they do not own a smartphone with internet and data packages, are pregnant, surgery is scheduled after the 9-month recruitment window, currently participating in an existing nutrition intervention study or those unable/unwilling to understand and/or follow the study protocol.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Our primary outcome will be feasibility, determined by achieving all three of the following: <br>(1)30 participants recruited <br>(2)>=80% of participants receiving the intervention for at least 4 weeks <br>(3)>=80% of participants achieving intervention adherence <br>[Participants will be deemed adherent if they have completed at least 75% of the prescribed food and beverage recording days using the mFR trademark app at 0 and 4 weeks before surgery and 6 weeks after surgery. Complete recording days will be defined as at least one meal recorded in a day. At the conclusion of the study.]
- Secondary Outcome Measures
Name Time Method Change in vegetable intake[mFR trademark app Baseline, Week 4 (pre-surgery) and Week 6 (post-surgery)];Change in overall diet quality[14-item Mediterranean Diet Adherence Screener Baseline, Week 4 (pre-surgery) and Week 6 (post-surgery)]