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'A Profile of Physical Performance Variables in an Out-patient Adult Population With Narcolepsy'

'A Profile of Physical Performance Variables in an Out-patient Adult Population With Narcolepsy'

Status
Suspended
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04419792
Enrollment
70
Registered
2020-06-05
Start date
2019-10-15
Completion date
2020-09-30
Last updated
2020-06-05

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

Conditions

Hypersomnolence, Narcolepsy, Narcolepsy 1, Narcolepsy and Hypersomnia, Narcolepsy Type 1, Narcolepsy With Cataplexy, Narcolepsy Without Cataplexy

Keywords

Physical performance, Cardiopulmonary fitness, Muscle strength, Muscle endurance, Quality of life, Physical activity

Brief summary

Narcolepsy is a sleep disorder characterised by excessive daytime sleepiness and significantly impacts quality of life. People with narcolepsy demonstrate many potential barriers to being physically active, such as sleepiness and social isolation. Very little is known about how physical performance variables may be affected and influence disease experience in people with narcolepsy. This study aims to profile the physical fitness and physical functioning variables of adults with narcolepsy and to explore the relationship between physical variables, quality of life, symptom severity and disease experience in this cohort.

Detailed description

This study aims to profile the physical functioning variables of people with narcolepsy attending an outpatient clinic at St. James's Hospital. This will be accomplished by ascertaining the cardiopulmonary fitness, physical activity, and muscle strength and endurance of this population. Secondary objectives of this study will be to explore the relationship between physical performance indices and sleep quality, functional ability and quality of life in this population.

Interventions

OTHERAssessment of physical performance variables

Other: Assessment of physical performance indices using the following outcome measures: Cardiopulmonary fitness: YMCA submaximal bike test Upper Body: ACSM press up test, Dynamometry Lower body: Wall squat test, Countermovement jump test

Sponsors

St. James's Hospital, Ireland
CollaboratorOTHER
University of Dublin, Trinity College
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years

Inclusion criteria

1. Patients diagnosed with narcolepsy type 1 or type 2 based on the International Classification of Sleep Disorders, third edition (ICSD-3) criteria for at least 6 months - diagnosis for at least 6 months will ensure that initial fluctuations due to likely starting on new drug regimen are relatively stable. 2. Eligibility screened and agreement of the participant's treating clinician in Narcolepsy out-patient clinic of St. James's Hospital that he/she can participate - to ensure that as per General Data Protection Regulation guidelines that the treating clinician eligibility screens rather than the physiotherapy study researcher. 3. Patients aged ≥18 to \<65 years at the time of obtaining informed consent - as patients \>18 years will not been seen in this centre, and patients \>65 years may have age-related changes in cardiovascular fitness and physical activity which may be difficult to separate from those pertaining to narcolepsy diagnosis. 4. Able to understand English - as questionnaires will necessitate a sufficient level of English for completion.

Exclusion criteria

1. Patients with sleep disorders other than narcolepsy (e.g., moderate to severe sleep apnea syndrome, moderate to severe periodic limb movement disorder) - so results are not diluted by including conditions other than narcolepsy. 2. Any medical contraindication to exercise of moderate intensity and short duration including but not limited to cardiovascular or respiratory conditions, morbid obesity, and severe osteoarthritis of the lower extremities - as these conditions would preclude ability to conduct physical test battery. 3. Confirmed pregnancy - people with an advanced pregnancy may score differently on physical functioning/performance tests, people with a confirmed pregnancy will be excluded from study participation to limit bias. 4. Dementia or significant cognitive impairment or psychiatric illness that would preclude ability to participate in study.

Design outcomes

Primary

MeasureTime frameDescription
Measurement of physical activity7 daysActigraphy will be used to objectively measure physical activity and sedentary behaviour. Participant will be required to wear the actigraph around their waist during all waking hours except during swimming or bathing, and then send back to assessor in return-addressed envelopes.
Measurement of oxygen uptake during cardiopulmonary exercise testing (% predicted)30 minutesThe submaximal Young Men's Christian Association (YMCA) exercise test utilises the relationship between workload and heart rate to predict maximal oxygen consumption. Provides indication of cardiopulmonary fitness.
Measurement of grip strength15 minutesObjective measure of grip strength of the dominant and non-dominant hands, and will provided indication of how grip strength compares to age and gender-matched norms. Dynamometry will be used to asses muscle strength of the upper limb.
Measurement of upper limb endurance10 minutesThe American College of Sports Medicine Press Up Test will be used to objectively measure muscular endurance of the upper limb. Identifies the maximum number of press ups that the participant can perform before failure.
Measurement of lower limb endurance10 minutesThe wall sit test will be used to objectively measure lower limb endurance. Measures the duration a participant can maintain a wall sit until failure.
Measurement of lower limb power.10 minutesThe Countermovement Jump Test will be used to objectively measure lower limb power. This test measures both jump height and peak power achieved by participants.

Secondary

MeasureTime frameDescription
Subjective measure of Health-Related Quality of Life10 minutesHealth-related quality of life will be subjectively assessed using the Short Form-36 questionnaire (Generic).
Subjective measure of Health-Related Quality of Life (sleep-disorder-specific)10 minutesHealth-related quality of life will be subjectively assessed using the Functional Outcomes of Sleep Questionnaire questionnaires
Subjective measure of symptom severity10 minutesSymptom severity will be subjectively assessed through use of the Narcolepsy Severity Scale.
Subjective measure of daytime sleepiness5 minutesDaytime sleepiness will be subjectively assessed through use of the Epworth Sleepiness Scale.
Subjective measure of physical activity5 minutesPhysical activity levels will be subjectively assessed through use of Physical Activity Vital Sign questionnaire.
Subjective measure of sedentary behaviour5 minutesSedentary behaviour levels will be subjectively assessed through use of Sedentary Behaviour Questionnaire.

Countries

Ireland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026