Development and Impact of a Nutrition Supplement and Nutrition Education on Patient Acceptance and Outcomes in Spine Surgery
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 98
- Locations
- 1
- Primary Endpoint
- Number of participants in each group with changes in PROMIS global and food frequency questionnaire.
Study Overview
Brief Summary
The goal of this interventional study is to learn if having 15 minutes of surgery related nutrition education changes the food choices participants make during the time right before and after a spine surgery in participants who have a surgery with Dr. John Edwards. The main questions it aims to answer are:
- Does nutrition education at a participant's preoperative appointment help them choose healthier foods and drinks that help their recovery from surgery?
- Does choosing to drink some extra nutrients before and after surgery help participants feel better and make it easier to have other foods and liquids after surgery? Researchers will compare participants getting extra education with those in a control group who have normal instructions from the clinic to see if extra education makes a difference in people's food choices. Researchers will also look at how well participants do with the extra nutrition they get before and after surgery, and if choosing to include it changes with the extra education.
Participants will:
- Complete 2 surveys (PROMIS global and food frequency) at both their preoperative and postoperative appointments
- Complete one survey 2 days after their surgery asking about how well they did with liquids and solid foods in the 24 hours after surgery
- Choose whether or not they decide to have a drink with extra nutrients before and after surgery, and let the researchers know what they chose.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Adult (18+ years of age)
- •Patient of Dr. John Edwards undergoing spine surgery
- •Patient is willing and able to complete all study requirements, including any education and follow up appointments
Exclusion Criteria
- •Under 18 years of age or pregnant
- •Known allergies or intolerances to any supplement ingredients
- •Patients deemed medically unstable by Dr. Edwards
- •Patients with uncontrolled diabetes, as identified as Hemoglobin A1C>7.5
- •Patients unwilling or unable to complete all study requirements including any education and follow up appointments
Arms & Interventions
Nutrition education
Participants randomized to this group will receive an additional 15 minutes of nutrition education focused on nutrition for surgical recovery. They will be offered an additional nutrition beverage if they choose it.
Intervention: nutrition education (Behavioral)
Control group with typical clinic education and care
Participants randomized to this group will receive typical clinic education and care. They will be offered an additional nutrition beverage if they choose it.
Outcomes
Primary Outcomes
Number of participants in each group with changes in PROMIS global and food frequency questionnaire.
Time Frame: The study starts at the preoperative visit, typically 2 weeks prior to surgery, and ends at the first postoperative visit, which is typically 4 weeks after surgery for a total study duration of about 6-7 weeks.
At both the preoperative and postoperative visits, participants will be given PROMIS Global and food frequency questionnaires.
Secondary Outcomes
- Number of participants with treatment-related adverse events of nausea and vomiting as assessed by CTCAE v4.0.(Total study duration is about 6-7 weeks from preoperative to initial postoperative visit, with this outcome measure being addressed 2 days following surgery.)
Investigators
Jennifer Bowden
Director of Research
Summit Brain,Spine,and Orthopedics