Under the NDIS, a restrictive practice is any practice or intervention that restricts the rights or freedom of movement of a person with disability. The NDIS Commission identifies five regulated restrictive practices:
No regulated restrictive practice can be used by an NDIS provider without proper authorisation. The requirements vary by state and territory, as authorisation frameworks are still transitioning to national consistency. Generally:
The specific authorising bodies and processes vary by jurisdiction. Check the NDIS Commission website for the current requirements in your state or territory.
An unauthorised restrictive practice must be reported to the NDIS Commission within 5 business days. Repeated unauthorised use can result in compliance action, conditions on registration, or deregistration.
For any BSP that includes a regulated restrictive practice, the plan must:
Every time a restrictive practice is used, it must be documented in the incident or behaviour record. Required documentation includes:
Providers must also report to the NDIS Commission at least quarterly on the use of regulated restrictive practices. The Commission provides specific templates for this reporting.
PRN medication — medication given as needed for behaviour management rather than as a prescribed treatment for a diagnosed condition — is classified as chemical restraint under the NDIS. It requires authorisation and documentation just like physical or environmental restraint. This is frequently misunderstood. If staff are administering PRN medication to manage a participant's behaviour, that use must be documented each time and included in quarterly reporting.
Environmental restraint is the most frequently used and least understood regulated restrictive practice. Locking a fridge, restricting access to a participant's phone, limiting freedom to go to certain rooms — if done to manage behaviour, these are regulated restrictive practices requiring authorisation.
Providers sometimes implement these informally without realising they require BSP authorisation. If you are doing anything that restricts a participant's access to something because of behaviour, consult a Behaviour Support Practitioner about whether authorisation is needed.
Every authorised restrictive practice must have a reduction plan — a documented strategy for how the practice will be reduced and ultimately eliminated. The goal of positive behaviour support is to replace restrictive practices with skill-building, environmental modifications, and proactive strategies.
Annual BSP reviews must assess whether the reduction plan is working. If a restrictive practice has been in use for years without any reduction in frequency or intensity, the BSP needs to be revised.
CareIQ's incident module captures restrictive practice use within the behaviour record — type, duration, staff, outcome, and whether it was consistent with the authorised BSP. 2-month free trial, no setup fee.
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