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A Lifestyle Intervention Program to treat Mild to Moderate Obstructive Sleep apnoea

A Diet and Exercise Program to Improve Sleep-Disordered Breathing, lose weight and improve fitness in patients with Obstructive Sleep Apnoea

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12606000284561
Acronym
nil
Enrollment
10
Registered
2006-07-05
Start date
2006-04-01
Completion date
Unknown
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

Subjects with mild to moderate obstructive sleep apnoea will be invited to participate in a supervised 4-month diet and exercise program. We will measure daytime function, quality of life and severity of sleep-disordered breathing before and after the study, and in addition will followup subjects for 12 months after they complete the active intervention protocol.

Interventions

The following interventions are implemented together for 4 months: 1. Diet - using very low energy liquid meal replacement (Optifast) in combination with low fat and low carbohydrate meals. 2. Exercise - both aerobic using exercise bikes and resistance using weights in a hospital gym, as well as at home. The hospital based sessions are for 40 minutes to 1 hour, 3 times each week for 8 weeks then once each week for 8 weeks. In addition, subjects are asked to exercise at home for 30-60 minutes on

The following interventions are implemented together for 4 months: 1. Diet - using very low energy liquid meal replacement (Optifast) in combination with low fat and low carbohydrate meals. 2. Exercise - both aerobic using exercise bikes and resistance using weights in a hospital gym, as well as at home. The hospital based sessions are for 40 minutes to 1 hour, 3 times each week for 8 weeks then once each week for 8 weeks. In addition, subjects are asked to exercise at home for 30-60 minutes on the days that they do not attend the hospital gym. There are no drugs involved.

Sponsors

Institute for Breathing and Sleep
Lead SponsorOther

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

AHI at least 10waist circumference at least 95cm in females, 100cm in males.

Exclusion criteria

Physical or psychological co-morbiditiesInability to exerciseDietary restrictionsInsulin requiring diabetesRenal or liver disease.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026