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As the year comes to a close, many OTs are feeling stretched. Illness, client demand, school schedules and end-of-year fatigue all shape the workload long before the NDIS is even factored in. When you add shifting guidelines, slow processes and decisions that seem to change without warning, it’s clear why many practitioners are questioning how to keep their work sustainable.
A new NDIA inquiry and why it matters
A parliamentary inquiry into the administration of the NDIA has been announced, with submissions due in January 2026. Its scope includes financial sustainability, regulatory performance and how the agency oversees compliance and reporting.
While this can feel removed from day-to-day clinical work, inquiries of this scale influence the policies and operational rules that eventually shape practice. They also offer a pathway to highlight recurring systemic issues rather than isolated individual cases. Many OTs, however, find the terms of reference vague, which makes it difficult to know what kind of feedback is genuinely useful.
Despite that uncertainty, one theme dominates in almost every OT’s experience…
Inconsistency across decisions and processes
Inconsistency remains the issue practitioners raise most often. The scheme no longer resembles the “half-built plane” analogy from its early years. Instead, it feels like a fully built aircraft whose destination keeps shifting.
Practically, this means similar requests can produce wildly different outcomes. Sensory equipment may be approved under core funding for one child but rejected for another. Progress reports may be viewed as essential in one region yet unnecessary in another. Even assistive technology requests that appear to match published pathways can be knocked back for technical reasons that feel arbitrary.
For example, a vision-adapted induction cooktop designed to replace an unsafe gas system may be rejected under the replacement pathway because it requires installation, forcing OTs to reposition the request as a minor home modification instead. These inconsistencies are compounded by the fact that some Operational Guidelines have not been updated in several years, leaving practitioners expected to comply with rules that do not always align with current practice.
This complexity makes it difficult for OTs to provide clear guidance to families, and unrealistic to expect that professionals can “just know the rules” when the rules behave unpredictably across teams, regions and time.
Change of circumstances and the new threshold for risk
Change of circumstances processes have been increasingly slow, and recent legislative updates have raised the threshold for acceptance. It is no longer enough to demonstrate increased need. There must now be explicit evidence that the participant’s health, safety or wellbeing is at risk if the plan is not reviewed.
For adults, clear risks may include missed medication, unsafe personal care, housing instability or unmonitored behaviours. In paediatrics, this is more complex. When a parent becomes unwell, dies or can no longer provide care, the remaining caregiver typically absorbs far more support than is sustainable. A child’s needs may appear to remain met, but only through significant sacrifice by the caregiver.
OTs face the ethical challenge of needing to describe these pressures clearly enough to justify support while also protecting families from unnecessary scrutiny. This requires sensitive, precise documentation that identifies the unmet need that emerges when caregiver capacity changes, and links this directly to the child’s health, safety and wellbeing.
The emotional load of review and tribunal processes
More NDIS decisions are progressing to external review, and many OTs are being drawn into tribunal processes despite having no training in giving evidence. The tribunal’s task is to determine whether the NDIA’s decision was legally correct, yet many therapists feel personally scrutinised when asked to justify their assessment or clinical reasoning.
In theory, an OT’s role is straightforward: explain the assessment, reasoning and recommendations. In reality, practitioners report uncertainty about preparation, what can be billed, how to answer targeted questions and what their legal obligations are. The emotional strain is significant, especially when paired with the desire to support families through stressful disputes.
Without clearer processes or consistent communication, this part of the system risks contributing to burnout among already stretched clinicians.
Using evidence and case law without becoming overwhelmed
Some therapists are beginning to reference tribunal decisions in their reporting, particularly in complex areas such as specialist disability accommodation. These decisions can be powerful when they clarify how legislation must be interpreted, especially where NDIA policy and practice do not align.
However, tribunal documents are lengthy and technical, and older decisions often relate to supports no longer considered part of the NDIS. Expecting clinicians to stay across an expanding body of case law is unrealistic. Shared resources that provide plain-language summaries and organise decisions by support type would be far more sustainable.
Until such tools are widely available, OTs need to remain selective about which decisions they reference and focus on those that are recent, relevant and legally aligned with current legislation.
What AI offers – and what it cannot replace
AI has quietly become part of many OTs’ workflows. It is particularly useful for non-billable or background tasks such as summarising supervision sessions, structuring report sections or organising information. It can also improve the clarity of written work and reduce cognitive load during busy periods.
Its limits, however, are clear. AI still misquotes transcripts, mixes up names or roles, and occasionally produces inaccurate information. It must be carefully reviewed. Because of this, AI is not likely to increase KPIs in any meaningful way. The time it saves is mostly time that clinicians were never billing for in the first place.
AI is best understood as a tool that supports clarity, quality and sustainability rather than a way to increase billable output.
Key takeaways for OTs
• Inconsistency across regions and decisions remains the biggest systemic challenge and often cannot be resolved at the individual clinician level.
• Change of circumstances requests must now clearly demonstrate health, safety or wellbeing risk, not just increased need or carer burden.
• In paediatrics, documenting unmet need after changes in caregiver capacity requires sensitivity, clarity and careful risk framing.
• When involved in review or tribunal processes, OTs are there to explain their reasoning rather than decide the outcome, and clearer guidance is essential.
• Tribunal decisions can strengthen recommendations, but only recent and relevant cases should be used.
• AI supports documentation quality and reduces administrative load but does not replace clinical judgement or meaningfully increase KPIs.
By Sarah Collison, Nikki Cousins and Alyce SvenskAs the year comes to a close, many OTs are feeling stretched. Illness, client demand, school schedules and end-of-year fatigue all shape the workload long before the NDIS is even factored in. When you add shifting guidelines, slow processes and decisions that seem to change without warning, it’s clear why many practitioners are questioning how to keep their work sustainable.
A new NDIA inquiry and why it matters
A parliamentary inquiry into the administration of the NDIA has been announced, with submissions due in January 2026. Its scope includes financial sustainability, regulatory performance and how the agency oversees compliance and reporting.
While this can feel removed from day-to-day clinical work, inquiries of this scale influence the policies and operational rules that eventually shape practice. They also offer a pathway to highlight recurring systemic issues rather than isolated individual cases. Many OTs, however, find the terms of reference vague, which makes it difficult to know what kind of feedback is genuinely useful.
Despite that uncertainty, one theme dominates in almost every OT’s experience…
Inconsistency across decisions and processes
Inconsistency remains the issue practitioners raise most often. The scheme no longer resembles the “half-built plane” analogy from its early years. Instead, it feels like a fully built aircraft whose destination keeps shifting.
Practically, this means similar requests can produce wildly different outcomes. Sensory equipment may be approved under core funding for one child but rejected for another. Progress reports may be viewed as essential in one region yet unnecessary in another. Even assistive technology requests that appear to match published pathways can be knocked back for technical reasons that feel arbitrary.
For example, a vision-adapted induction cooktop designed to replace an unsafe gas system may be rejected under the replacement pathway because it requires installation, forcing OTs to reposition the request as a minor home modification instead. These inconsistencies are compounded by the fact that some Operational Guidelines have not been updated in several years, leaving practitioners expected to comply with rules that do not always align with current practice.
This complexity makes it difficult for OTs to provide clear guidance to families, and unrealistic to expect that professionals can “just know the rules” when the rules behave unpredictably across teams, regions and time.
Change of circumstances and the new threshold for risk
Change of circumstances processes have been increasingly slow, and recent legislative updates have raised the threshold for acceptance. It is no longer enough to demonstrate increased need. There must now be explicit evidence that the participant’s health, safety or wellbeing is at risk if the plan is not reviewed.
For adults, clear risks may include missed medication, unsafe personal care, housing instability or unmonitored behaviours. In paediatrics, this is more complex. When a parent becomes unwell, dies or can no longer provide care, the remaining caregiver typically absorbs far more support than is sustainable. A child’s needs may appear to remain met, but only through significant sacrifice by the caregiver.
OTs face the ethical challenge of needing to describe these pressures clearly enough to justify support while also protecting families from unnecessary scrutiny. This requires sensitive, precise documentation that identifies the unmet need that emerges when caregiver capacity changes, and links this directly to the child’s health, safety and wellbeing.
The emotional load of review and tribunal processes
More NDIS decisions are progressing to external review, and many OTs are being drawn into tribunal processes despite having no training in giving evidence. The tribunal’s task is to determine whether the NDIA’s decision was legally correct, yet many therapists feel personally scrutinised when asked to justify their assessment or clinical reasoning.
In theory, an OT’s role is straightforward: explain the assessment, reasoning and recommendations. In reality, practitioners report uncertainty about preparation, what can be billed, how to answer targeted questions and what their legal obligations are. The emotional strain is significant, especially when paired with the desire to support families through stressful disputes.
Without clearer processes or consistent communication, this part of the system risks contributing to burnout among already stretched clinicians.
Using evidence and case law without becoming overwhelmed
Some therapists are beginning to reference tribunal decisions in their reporting, particularly in complex areas such as specialist disability accommodation. These decisions can be powerful when they clarify how legislation must be interpreted, especially where NDIA policy and practice do not align.
However, tribunal documents are lengthy and technical, and older decisions often relate to supports no longer considered part of the NDIS. Expecting clinicians to stay across an expanding body of case law is unrealistic. Shared resources that provide plain-language summaries and organise decisions by support type would be far more sustainable.
Until such tools are widely available, OTs need to remain selective about which decisions they reference and focus on those that are recent, relevant and legally aligned with current legislation.
What AI offers – and what it cannot replace
AI has quietly become part of many OTs’ workflows. It is particularly useful for non-billable or background tasks such as summarising supervision sessions, structuring report sections or organising information. It can also improve the clarity of written work and reduce cognitive load during busy periods.
Its limits, however, are clear. AI still misquotes transcripts, mixes up names or roles, and occasionally produces inaccurate information. It must be carefully reviewed. Because of this, AI is not likely to increase KPIs in any meaningful way. The time it saves is mostly time that clinicians were never billing for in the first place.
AI is best understood as a tool that supports clarity, quality and sustainability rather than a way to increase billable output.
Key takeaways for OTs
• Inconsistency across regions and decisions remains the biggest systemic challenge and often cannot be resolved at the individual clinician level.
• Change of circumstances requests must now clearly demonstrate health, safety or wellbeing risk, not just increased need or carer burden.
• In paediatrics, documenting unmet need after changes in caregiver capacity requires sensitivity, clarity and careful risk framing.
• When involved in review or tribunal processes, OTs are there to explain their reasoning rather than decide the outcome, and clearer guidance is essential.
• Tribunal decisions can strengthen recommendations, but only recent and relevant cases should be used.
• AI supports documentation quality and reduces administrative load but does not replace clinical judgement or meaningfully increase KPIs.

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