slaappatroon Sleeppattern
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: mild intellectual disability
Exclusion criteria
Exclusion criteria: People with spasms. people with known destructive behavior directed at property
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Participants wear the actiwatch for seven consecutive days. In this period, every morning the participant fills in the SSR-ID. At the end of the week, the Actiwatch and the answers of the SSR-ID will be collected by the researcher and the participant will be asked to evaluate their experience with the SSR-ID, by answering the questions on the last pages included to the SSR-ID. Then, data from the Actiwatch will be extracted using the Sleep Analysis Software (see above). For the questionnaire, a sumscore of each item is derived and a mean or median is calculated for respectively normal and non-normal distributions. These scores eventually are correlated to the sumscores of the actiwatch parameters Actiwatch: • Time in bed (TIB); total time the participants spend in bed. • Sleep onset latency (SOL); the interval between bedtime and sleep start. • Total sleep time (TST) • The time awake between sleep start en sleep end (WASO) • The percentage of time asleep during the total time in bed (sleep efficiency, SE) • Interval between sleep and get-up time (get-up time latency, GTL). Sleep Self Report Questionnairre: The development of the questions will be part of this research project. The answers to the final questions can be correlated against parameters of the actiwatch. Each item on the questionnaire will be answered for 7 times (7 consequetive days). We will use a weigthed mean of each item in our analysis. For details, see the questionnaire in the protocol's attachment. | — |
Secondary
| Measure | Time frame |
|---|---|
| inapplicable | — |
Countries
Netherlands
Outcome results
None listed