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Is two days of intermittent fasting per week a feasible weight loss approach in obese male war veterans? A pilot study.

For obese male war veterans aged between 55-75 years, will two days of intermittent fasting per week when compared with a standard 500kcal reduced diet promote more weight loss.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000396628
Enrollment
25
Registered
2014-04-10
Start date
2014-05-20
Completion date
2015-04-07
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This pilot study aims to determine whether the intermittent fasting approach leads to greater weight loss and greater improvements in blood sugar, cholesterol and blood pressure than a standard low energy diet in obese male war veterans. Our primary objective is to determine whether obese, male war veterans who undertake intermittent fasting (5:2 method) achieve at least 5% weight loss in six months.

Interventions

Intermittent Fasting Group Participants will be asked to follow a diet containing only 500kcal for two non-consecutive days per week and eat normally (unrestricted but encouraged to follow healthy eating guidelines) on the other five days for 6 months. Participants will be taught how to count calories and recieve dietary advice regarding healthy eating and food portions (as per Australian Guide to Healthy Guidelines). A calorie counting book will be provided. They will receive regular dieteti

Intermittent Fasting Group Participants will be asked to follow a diet containing only 500kcal for two non-consecutive days per week and eat normally (unrestricted but encouraged to follow healthy eating guidelines) on the other five days for 6 months. Participants will be taught how to count calories and recieve dietary advice regarding healthy eating and food portions (as per Australian Guide to Healthy Guidelines). A calorie counting book will be provided. They will receive regular dietetic review and monitoring during the first 3 months (baseline, 2 weeks, 4 weeks, 8 weeks and 12 weeks) and minimal contact during the remaining 3 months. The initial session with the dietitian at baseline will be 45 minutes in duration and all subsequent reviews will be 30 minutes in duration. Participants will have biochemical markers (fasting lipids and fasting glucose), biological impedence (to estimate percentage body fat), waist circumference and blood pressure taken at baseline, 3 months and 6 months. They will also complete a food frequency questionnaire and a validated quality of life questionnaire (AQoL 8D scale) at these times. Participants will have weight monitored and will be questioned about their compliance with the diet at all reviews (baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks and 6 months). In order to promote compliance, participants will be provided with sample recipes and will be able to contact the study dietitian during business hours for further clarification or dietary advice.

Sponsors

Lauren Le Fevre
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Outcomes Assessor)

Eligibility

Sex/Gender
Male
Age
55 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

Male war veteran aged 55-75 years old Have a BMI greater than or equal to 30kg/m2 Have a stable body weight (+/- 5% body weight change in the last 3 months) Have own local doctor who is aware of the health issues of the participant

Exclusion criteria

Have a medical contraindication (e.g. active cancer, unstable diabetes, insulin dependent diabetes, end stage renal failure) Have a high alcohol intake (greater than 28 standard drinks per week) Are taking antpsychotic medication associated with weight gain (Mirtazapine, Olanzapine, Clozapine)

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026