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Activity to reduce obstructive sleep apnoea

The implementation of a physical activity intervention in adults with obstructive sleep apnoea over the age of 50 years: a feasibility uncontrolled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11016312
Enrollment
10
Registered
2020-07-21
Start date
2017-08-08
Completion date
Unknown
Last updated
2020-08-24

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

Conditions

Obstructive sleep apnoea Nervous System Diseases Sleep apnoea

Interventions

Overnight screening for Obstructive Sleep Apnoea (OSA) indicates eligible participants with an Apnoea Hypopnoea Index (AHI) score greater than 15 who are then invited to take part in the intervention.

Sponsors

University of Birmingham
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult manual workers 2. Aged between 50 and 69 years old 3. No previous diagnosis or treatment for obstructive sleep apnoea 4. No history of chest pain during exercise or heart trouble 5. Employed for at least the previous 3 months or longer

Exclusion criteria

Exclusion criteria: 1. Younger than 50 or older than 69 years old 2. Unemployed or employed for less than 3 months 3. Previous diagnosis or treatment for obstructive sleep apnoea 4. History of chest pain during exercise or heart trouble

Design outcomes

Primary

MeasureTime frame
Feasibility of increasing the duration and intensity of weekly physical activity: participant compliance and adherence to the intervention measured using daily self-reporting via text messaging, objectively confirmed using accelerometry for seven consecutive days during week 6 and week 12

Secondary

MeasureTime frame
1. Physical activity measured subjectively using the short form International Physical Activity Questionnaire (IPAQ) at baseline and 12 weeks 2. Physical activity measured objectively using accelerometry at baseline, 6 weeks and 12 weeks 3. The presence and severity of Obstructive Sleep Apnea (OSA) evaluated using the Apnoea/Hypopnoea Index (AHI) using a domiciliary testing device (ApneaLink Air) at baseline and 12 weeks 4. Anthropometric measurements: BMI (kg/m2) and weight and body fat percentage measured using bioelectrical impedance at baseline and 12 weeks

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 26, 2026