Task Completion Time
Time to navigate from start to goal chamber
Multi-chamber system for high-throughput spatial learning assessment.
Metrics automatically extracted by ConductVision.
Time to navigate from start to goal chamber
Incorrect door attempts per trial
Trial-over-trial error reduction slope
Error variance on fixed sequences indexing reliability
Latency to respond to auditory or visual cues
Proportion of trials with correct door selection at each decision point
Error difference between novel and fixed sequences — learning vs retrieval
Repeated incorrect choices at the same decision point
Error rate by position in the door sequence — primacy/recency patterns
Time between successive door choices within a trial
Performance improvement when retested on previously learned sequences
The Repeated Acquisition and Performance Chamber automates assessment of spatial learning by requiring rodents to navigate interconnected compartments, choosing the correct door at each decision point. The acquisition phase uses a novel sequence each session while the performance phase uses a fixed sequence, enabling within-subject dissociation of new learning from established memory.
ConductVision integrates with RAPC's electronic sensors for automated error scoring across up to 16 simultaneously running chambers. RAPC is widely used in neurotoxicology, pharmacological screening, and aging research.
| Parameter | Description | Default |
|---|---|---|
| Number of Chambers | Interconnected compartments in sequence | 3–4 |
| Chamber Size | Individual compartment dimensions | 30 × 25 × 25 cm |
| Door Type | Automated sliding doors at decision points | Motorized guillotine |
| Acquisition Sequence | Door sequence changes each session (novel learning) | Random per session |
| Performance Sequence | Fixed door sequence across sessions (established memory) | Constant |
| Trials per Session | Number of complete runs per session | 10–20 |
| Session Duration | Maximum time per session | 30 min |
| Reward | Food reward in the goal chamber | 45 mg sucrose pellet |
| Food Deprivation | Body weight maintained at | 85–90% free-feeding |
| ITI | Inter-trial interval | 10–15 s |
| Simultaneous Chambers | Number of RAPC units run in parallel | Up to 16 |
Impaired new learning — failure to acquire novel sequences indicates hippocampal or prefrontal dysfunction.
Degraded established memory — errors on the fixed sequence suggest memory retrieval or consolidation deficit.
Slowed learning — flatter error reduction slope across trials, common in neurotoxicant exposure models (lead, mercury).
Cognitive inflexibility — repeated incorrect choices at the same decision point indicate perseverative behavior.
Dissociation — acquisition errors increase while performance errors remain stable, indicating new learning deficit only.
Inconsistent retrieval — high error variance on the fixed sequence suggests unreliable memory access.
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