ELECtric Tibial Nerve Stimulation to Reduce Incontinence in Care Homes (ELECTRIC)
Urinary Incontinence
About this trial
This is an interventional treatment trial for Urinary Incontinence
Eligibility Criteria
Inclusion Criteria:
Care home residents:
- with self or staff reported UI of more than once/week
- who use the toilet or toilet aid for bladder evacuation with or without assistance
- who wear absorbent pads to contain UI.
Exclusion Criteria:
Care home residents:
- with an indwelling urinary catheter
- residents with UTI
- residents with PVRU volume more than 300ml
- residents with a cardiac pacemaker
- residents with treated epilepsy
- residents with bilateral leg ulcers
- residents with pelvic cancer
- residents on the palliative care register
Sites / Locations
- Glasgow Caledonian University
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
TPTNS Intervention
Sham stimulation
Transcutaneous posterior tibial nerve stimulation (TPTNS) delivered in 30 minute sessions twice weekly over a 6 week period. The tibial nerve, which lies immediately posterior to the medial malleolus will be stimulated electrically using a portable TENS machine and two surface electrodes. The cathode electrode will be positioned behind the medial malleolus and the anode 10cm cephalad to it. Standardised stimulation parameters will be applied at 10 Hz frequency, 200µs-1 pulse width in continuous mode and stimulation intensity (mA-1) will be adjusted on a session-by-session basis according to individual resident comfort levels.
Sham stimulation comprises low intensity, sub-clinical stimulation of the lateral sub-malleolar area, positioned specifically on the lateral aspect to avoid the tibial nerve, which runs close to the skin surface behind the medial malleolus. The stimulation parameters are identical to the TPTNS stimulation other than the intensity of the current which will be set at 4mA, rather than adjusted individually as it is in the TPTNS intervention group. The current will be initially increased until the resident reports feeling some sensation following which the current will be reduced down to 4mA. All residents will be informed that they may not feel anything with this intervention and that this is quite normal.