In case anybody currently looking comes across this post...
A few RNA-Seq QC tools will detect whether a run is strand-specific. For example, the infer_experiment.py script in the following claims to do this (never used this myself, so can't vouch for it):
This image could help. https://galaxyproject.org/tutorials/rb_rnaseq/stranded_result.png
In stranded example reads are clearly stratified between the two strands
Of course, you need to perform the alignments, get the BAM file and visualize it in any of the software available (SeqMonk, RNAseqViewer, IGB, etc)