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Life-style Changes in Obstructive Sleep Apnea

Health Behaviour Modifications in Obstructive Sleep Apnea. Tailored Behavioural Medicine Strategies to Promote Physical Activity and Weight Loss.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01102920
Enrollment
86
Registered
2010-04-13
Start date
2010-05-31
Completion date
2014-09-30
Last updated
2017-11-08

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

Conditions

Obesity, Sleep Apnea, Obstructive

Keywords

Obstructive sleep apnea, Obesity, Behavioural medicine, Physical therapy, Health behaviour change, Physical activity, Eating habits

Brief summary

The primary aim is to study whether a tailored behavioural medicine intervention addressing physical activity and eating habits have additional effects to continuous positive airways pressure (CPAP) in patients with moderate or severe obstructive sleep apnea syndrome (OSAS) combined with obesity. Direct everyday life consequences (see below) of OSAS are studied, as well as cognitive functions and ventilatory parameters. Long-term benefits will be examined in terms of quality of life and everyday life activity. Another aim is to study mechanisms of treatment effects, if any. The specific goals are: 1. To study changes in OSAS ventilatory parameters following a tailored behavioural medicine intervention addressing physical activity and eating habits (including CPAP) compared to regular CPAP-treatment 2. To study immediate and long-term effects on daytime sleepiness, attention and concentration, everyday life activity, quality of life following a tailored behavioural medicine intervention addressing physical activity and eating habits (including CPAP) compared to regular CPAP-treatment 3. To study associations of changes in metabolic parameters and systemic inflammation and physical activity level and adherence to CPAP-regimen respectively. 4. To identify mediators, moderators, and predictors of treatment effects, if any.

Detailed description

OSAS is characterised by loud snoring, upper airway obstruction, and occasional apnea during sleep. OSAS may affect at least 4% of the men and 2% of the women in middle-age. In Sweden, prevalence figures of 200 000 have been reported. The mechanisms behind OSAS is not fully explained but functionally impaired upper airways muscles, causing a reduction in tonic and phasic contraction during sleep, are proposed one key explanation. The reduced contractions cause partial or complete occlusion of airflow, which in turn cause oxygen desaturation and sleep fragmentation. Patients commonly report everyday life consequences including loud snoring, sleep disturbances, daytime sleepiness, reduced alertness and concentration, and involvement in motor vehicle accidents. Between 7% and 70% of patients suffer from depression and anxiety (figures vary extensively because of methodological differences in existing studies). Due to cardiovascular consequences, OSAS is also linked to hypertension, myocardial infarction, and stroke. Approximately 75% of patients with severe OSAS carry overweight. First line measures recommended for OSAS are conservative including lifestyle modifications, CPAP, and oral appliances. Current state-of-science concludes that CPAP is best possible evidence-based treatment. Despite the use of life style modification recommendations in terms of physical activity and weight loss in accepted guidelines of OSAS, randomised clinical trials supporting these recommendations are rare. Hence, the value of health behaviour modifications has yet to be established. Research within this area is therefore of major interest and urgency, which has motivated the present study design.

Interventions

BEHAVIORALBehavioural strategies to promote physical activity and weight loss

8-10 sessions, 2-4 booster sessions Behavioural protocol in seven steps to initiate, carry out and maintain health-enhancing physical activity and sound eating habits. Steps are standardized including: progressive goal setting, self-monitoring, functional behavioural analysis, skills training (basic and applied), generalization, and maintenance and relapse prevention. Content within each step is tailored to individual expectations and skills. Treatments are provided by a physical therapist and a dietician.

DEVICECPAP

CPAP-treatment as usual (during nights)

Sponsors

The Swedish Research Council
CollaboratorOTHER_GOV
Uppsala County Council, Sweden
CollaboratorOTHER_GOV
Uppsala University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Moderate or severe obstructive sleep apnea syndrome (AHI/DI\>15) * BMI\>30 * Literate in Swedish language

Exclusion criteria

* Physically active patients (walking, bicycling for more than 30 minutes per day,during more than 5 days per week) * Cardiovascular diseases including myocardial infarctions and stroke * Patients on waiting list for gastric by-pass

Design outcomes

Primary

MeasureTime frameDescription
Ventilatory parametersBaseline, immediate post-treatment, 18-month follow-upVentilatory monitoring at night. Oxygen saturation continuously measured by a pulse oximeter. The following parameters are analysed: * desaturation index * apnoea-hypnoea index * average oxygen saturation during sleep * minimum oxigen saturation * respiration * thoracic respiratory movements * snoring * heart rate * body position

Secondary

MeasureTime frameDescription
Attention and concentrationBaseline, immediate post-treatment, 18-month follow-up* COWAT * Repetition of figures from WAIS
Health-related quality of lifeBaseline, immediate post-treatment, 18-month follow-upSF-36
Patients' priorities of daily activities and participationBaseline, immediate post-treatment, 18-month follow-upThe Patient Goal Priority Questionnaire
Physical activityBaseline, immediate post-treatment, 18-month follow-up* Sensewear armband * Physical activity diary
Functional physical capacityBaseline, immediate post-treatment, 18-month follow-up6 minutes walking distance
Daytime sleepinessBaseline, immediate post-treatment, 18-month follow-upEpworths sleepiness scale
Self-efficacy and readiness to change behaviourBaseline, mid-treatment, immediate post-treatment, 18-month follow-up* Exercise self-efficacy scale * Self-efficacy for sound eating habits * Readiness to change behaviour
AnthropometricsBaseline, immediate post-treatment, 18-month follow-up* BMI * Waist measurement * Neck circumference
DepressionBaseline, immediate post-treatment, 18-month follow-upMADRS Depression scale
Fear of movementBaseline, mid-treatment, immediate post-treatment, 18-month follow-upSelected items from the Tampa Scale of Kinesiophobia
Blood sampleBaseline, immediate post-treatment, 18-month follow-up* CRP * TNF-alfa * lgF-1 * Hb * HbA1C * s-cholesterol, HDL, LDL, s-triglycerids * K, Na * Creatinin, Leptin, Sysozym, n-terminal pBNP
Eating behaviourBaseline, immediate post-treatment, 18-month follow-upDutch eating behaviour questionnaire

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026