TABLE 5.
Participants Displaying an Impairmenta | Participants with Urgency Provoked with Primary Testb | Participants with Urgency Relieved with Secondary Testc | |||||
---|---|---|---|---|---|---|---|
Movement/Positional Test | UFLUTSf n=21 |
Cong n=21 |
Ph | UFLUTSf n=21 |
Cong n=21 |
Ph | UFLUTSf n=21 |
Forward bend | 15 | 10 | <.21 | 2 | 0 | 0.49 | 3 |
Return from forward bend | 12 | 4 | 0.03 | 5 | 0 | 0.05 | 4 |
Single leg stancee | 21 | 10 | <.01 | 0 | 0 | 0.99 | 3 |
Sidelyinge | 21 | 12 | <.01 | 3 | 1 | 0.61 | 11 |
Participants Displaying a Positive Testd | Participants with Urgency Provoked during Testb | ||||||
Additional Clinical Testse | UFLUTSf n=21 |
Cong n=21 |
Ph | UFLUTSf n=21 |
Cong n=21 |
Ph | |
FADIR | 7 | 4 | 0.48 | 8 | 1 | 0.02 | |
FABER | 3 | 2 | 0.99 | 3 | 1 | 0.61 | |
Stork test | 17 | 6 | <.01 | ||||
Pubic symphysis palpation | 16 | 5 | <.01 | ||||
Hip ROM | 17 | 12 | 0.18 | ||||
External Rotation ROM | 2 | 0 | 0.50 | ||||
Internal Rotation ROM | 5 | 0 | <.01 |
Number of participants with any examiner-observed movement impairment in spine, pelvis or hip during primary test
Number of participants who reported same or worse bladder urgency during primary test compared to baseline
Number of participants who reported reduced bladder urgency with secondary test when compared to symptoms during the primary test
Number of participants with positive test (see Table 4)
Test performed bilaterally, participants only counted once regardless of if the phenomena occurred bilaterally
Participants with bothersome urgency and/or day/night frequency at least sometimes in the past 4 weeks
Participants without urgency and frequency symptoms
P≤ .05, values from Fisher’s exact test