None listed
Conditions
Brief summary
Given the wide spectrum of metabolic consequences post SCI in conjunction with age-related co- morbidities with increased life expectancy in recent years, it is imperative to implement timely and targeted risk modification strategies. There is evidence that dietary and lifestyle modifications minimise several CVD risk factors in individuals with SCI and good evidence in the role of physical activity in improving cardio-metabolic outcomes in the population. Therefore, this study aims to examine the association between diet quality on lipid profile and body weight of spinal cord injury patients. Hypothesis: Compliance with a Mediterranean style dietary pattern is associated with lower CVD risk in adults with SCI.
Interventions
Patients will be provided with dietary education and offered menu selection of food choices from a “cardio-diet”. Data will be collected at baseline, every 4 weeks during hospital stay and 6-8 weeks post discharge. Cardio-metabolic profile data collection include: Anthropometry – Height, body weight, waist circumference Biochemistry – Lipid profile (Total cholesterol, HDL, LDL, TG) fasting BGL, HbA1c, CRP, homocysteine, insulin resistance (HOMA-IR) Clinical – Body composition using bio-impedance spectroscopy (SFB7) and blood pressure Diet –A validated Food Frequency questionnaire (DHQ III) will be used to quantify pre-morbid/pre-hospital intake data. Dietary intake during admission will be measured using a 3-day food record, representing 2 weekdays and one weekend day. Diet quality will be assessed at each point using Mediterranean diet assessment tool (MEDAS). All recruited patients will be offered the “cardio-diet” menu in line with the Mediterranean diet, low saturated fat with high fruits and vegetables, low salt intake including wholegrains and legumes. Additionally, meals will be tailored using small, regular and large serves based on the energy requirements calculated using spinal cord injury specific guidelines. . Dietary intake will be measured using a 3-day food record, representing 2 weekdays and one weekend day. The form will be completed by either the patient/family and/or the nursing staff.Diet quality as well as compliance will be assessed at baseline and each check point during the intervention period using the validated 14-item Mediterranean Diet Assessment Tool (MEDAS) Education – 1 x 30 minute group session (week 2) and 2 x 15 minute duration one-on-one tailored nutrition education sessions of 15 minutes duration each at week 4 and week 8 with written handouts will be provided during the 12-week intervention period. Nutrition education will incorporate modules in line with social cognitive theory and protection motivation theory with behaviour change techniques including motivational interviewing, goal-setting and positive reinforcement/feedback in addition to self-monitoring of behaviour. Nutrition education handouts will bee purpose-designed, specifically for this study and education sessions are conducted by the accredited practicing dietitian at all times. All baseline markers will be tested at periodic intervals of 0, 4, 8, & 12 weeks except for body composition and biochemistry, which will be reviewed at baseline, 12 weeks and post discharge only. If patients are discharged home prior, follow-up will be completed in the community for that period. Community follow-up at ~6-8 weeks post discharge (as 18 weeks’ review or more depending on the time of discharge) will follow all discharges. The findings will be reported according to the STROBE statement.
Sponsors
Study design
Eligibility
Inclusion criteria
All adult inpatients admitted to the spinal injury rehabilitation unit, with or without existing CVD risk/disease at Royal Rehab consenting to participate will be included in this study.
Exclusion criteria
1. Community dwelling individuals with spinal cord injury and inpatients in acute care facilities will be excluded from this study. 2. Participants who decline or refuse to participate in the study. Refusal to participate in the study will in no way affect their treatment and these individuals will still receive regular services from the Nutrition and Dietetics team at the facility. These participants also have the liberty to opt for the cardo-diet choice, should they prefer even during non-enrolment into the study. 3. Patients with concurrent or a history of traumatic brain injury with cognitive impairment interfering with their ability to understand the requirements of the study. 4. Patients on enteral feeding or very low energy diet (e.g. Optifast) will be excluded. 5. Patients with grade 2 or above pressure injuries will be excluded. 6. Patients with a pacemaker, those who are either pregnant or breast-feeding will be excluded.