Chronic Kidney Diseases, Obesity
Conditions
Keywords
intermittent fasting, weight loss
Brief summary
This study proposes to investigate the acceptability and efficacy of intermittent VLED (5:2 diet) plus exercise, compared with the investigator's established Weight Management Programme (WMP), in obese patients with CKD, using feasibility study methodology. Patients will be invited to participate in the parallel arm, single blinded, randomised controlled feasibility study, and randomly allocated to 1 of 2 treatments for 6 months. The experimental arm involves an intermittent modified fasting regimen consisting of VLED (600 kcal/day) on 2 consecutive days, and 5 days each week on a modified diet to maintain an overall energy deficit of 600 kcal/day across the week (5:2 diet). The control arm will be the standard renal WMP with a continuous energy restricted diet aimed at reducing daily energy intake by 600 kcal/day. The feasibility outcomes are: recruitment rate \>50%; intervention retention rate at 6 months \>60%; dietary intervention compliance; and weight loss. Secondary outcomes include safety, body composition, proteinuria, lipids, blood pressure, and eating desire. Measurements will be made at baseline, midpoint, and twice at endpoint.
Interventions
BEHAVIORAL5:2 diet
very low energy diet (600 kcal/day) on 2 consecutive days of the week, and 5 days each week on an energy restricted diet to maintain a similar overall energy deficit of 600 kcal/day across the week (5:2 diet)
BEHAVIORALRenal Weight Management Programme
Dietary intervention includes a standard continuous energy restricted diet aimed at reducing daily energy intake by 600 kcal/day relative to their estimated total energy expenditure. In addition to the dietary intervention, the programme also includes personal exercise plans, optional pharmacotherapy (orlistat at standard dose), and development of personalised dietary and exercise goals using behavioural therapy techniques and motivational interviewing.
Sponsors
King's College Hospital NHS Trust
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
Study outcome measures performed by assessor blinded to treatment arm
Intervention model description
Parallel arm, single blinded, randomised controlled feasibility study
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* aged 18-75 years * KDIGO defined CKD (all categories) * BMI ≥30kg/m2 * able to provide written informed consent in English
Exclusion criteria
* pregnant or breastfeeding women * conservatively managed CKD stage 5 * palliative or active treatment for cancer * unstable chronic liver disease * type 1 diabetes and type 2 diabetes controlled with anti-hyperglycaemic medication * previous bariatric surgery * unable to provide written informed consent * significant psychiatric disorder or uncontrolled depression * participated in a weight management drug trial in the previous 3 months * uncontrolled epilepsy * alcohol or substance abuse
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Retention rate of at least 60% in the intervention group | 6 months | Patients attending at least 80% of monthly clinic visits, including the baseline and final study visits, and remaining compliant with the 2 consecutive days VLED throughout the 6 month intervention will be considered completers and count as being retained in the intervention group at 6 months. |
| Number of Adverse Events following intermittent very low energy diet | 6 months | record of all adverse events including but not limited to nausea, constipation and/or diarrhoea, dehydration, hypoglycaemia, lethargy & fatigue, headaches, gallstones and gout. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Weight change (kg) | 6 months | change in weight from baseline to 6 months |
| kidney function (eGFR ml/min CKD EPI equation) | 6 months | monitoring if estimated kidney function declines during the study or if symptomatic for dehydration. |
| Waist circumference (cm) | 6 months | change in waist circumference measured in cm at level of umbilicus |
| Body composition | 6 months | lean and fat mass (kg) estimated by bioelectrical impedance analysis |
| Exercise capacity - 6 minute timed walk test | 6 months | distance walked (m) in 6 minutes |
| Recruitment rate of at least 50% of potential participants meeting inclusion and exclusion criteria | 1 year | at least 50% of those meeting the referral criteria and are approached to participant, consent to participating in the study |
| Proteinuria | 6 months | urinary protein to creatinine ratio |
| Total Cholesterol | 6 months | plasma total cholesterol concentration |
| Triglycerides | 6 months | plasma triglycerides concentration |
| LDL cholesterol | 6 months | plasma LDL cholesterol concentration |
| HDL cholesterol | 6 months | plasma HDL cholesterol concentration |
| Exercise capacity - sit to stand 60 | 6 months | number (count) of sit to stand movements in 60 seconds |
| Compliance with dietary intervention from dietary records | 6 months | at least 70% compliance with prescribed diet |
Countries
United Kingdom
Outcome results
None listed