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ELECtric Tibial Nerve Stimulation to Reduce Incontinence in Care Homes (ELECTRIC)

Primary Purpose

Urinary Incontinence

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Transcutaneous posterior tibial nerve stimulation
Sham stimulation
Sponsored by
Glasgow Caledonian University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Incontinence

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Sham Comparator

Arm Label

TPTNS Intervention

Sham stimulation

Arm Description

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.

Outcomes

Primary Outcome Measures

Volume of UI leaked
Volume of UI leaked over a 24 hour period

Secondary Outcome Measures

Pad use
Number of pads used in 24 hours
PVRU volume
Post-void residual volume of urine scanned in bladder
PBBC
Patient Perception of Bladder Condition
FC-PBC
Family Carer Perception of Bladder Condition
S-PBC
Staff Perception of Bladder Condition
Resident DEMQOL
Resident perception of quality of life
Staff DEMQOL
Staff perception of quality of life
RUQ
Economic evaluation via a resource use questionnaire
Semi structured interviews with residents, carers and staff regarding the impact of experiences of the TPTNS intervention and any impact on quality of life
Exploration of the experiences of the TPTNS intervention from the perspectives of residents, family carers and care home staff.
Semi-structured interviews and focus groups with care home staff and managers regarding the potential for integrating TPTNS into routine care within care homes, long-term
Exploration of the factors affecting intervention implementation in the care home context and optimisation for sustainability

Full Information

First Posted
August 1, 2017
Last Updated
January 8, 2020
Sponsor
Glasgow Caledonian University
Collaborators
National Institute for Health Research, United Kingdom
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1. Study Identification

Unique Protocol Identification Number
NCT03248362
Brief Title
ELECtric Tibial Nerve Stimulation to Reduce Incontinence in Care Homes
Acronym
ELECTRIC
Official Title
ELECtric Tibial Nerve Stimulation to Reduce Incontinence in Care Homes: ELECTRIC
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 29, 2018 (Actual)
Primary Completion Date
December 30, 2019 (Actual)
Study Completion Date
June 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Glasgow Caledonian University
Collaborators
National Institute for Health Research, United Kingdom

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study aims to determine whether a programme of transcutaneous posterior tibial nerve stimulation (TPTNS) is a clinically effective treatment for urinary incontinence (UI) in care home residents and what the associated costs and consequences are.
Detailed Description
Urinary incontinence is a distressing and embarrassing condition that occurs in around 70% older people who live in nursing or residential care homes. It is common in those who have dementia as well as those with other medical conditions. Urinary incontinence has a major impact on an older person's dignity and quality of life and is linked to other health problems and relationship difficulties. It also affects a person's ability and willingness to socialise. There are not many options for treatment of urinary incontinence in older people, especially those with dementia. There are several drugs available but these can have unpleasant side-effects. Sometimes pelvic floor muscle exercises, or going to the toilet at regular intervals are tried but these can be difficult to do by those who find it hard to get around or have memory problems. They are also hard to maintain in the longer term and so older people who experience bladder leakage usually rely on the use of absorbent pads to hold the urine, rather than trying to treat the cause of the problem. Transcutaneous posterior tibial nerve stimulation (TPTNS) involves placing two sticky pads (surface electrodes) on a person's ankle and connecting these to a small, pocket sized electrical stimulator. This sends an electric pulse to the nerve near the ankle which also controls the bladder. Each treatment lasts half an hour and a total of twelve are given over a six week period. The treatment is similar to a TENS machine which is sometimes used for treating pain. It is a gentle pulsing and its strength is altered to suit the person and what is comfortable for them. TPTNS helps people with bladder leakage because it reduces the feeling of sudden urgency and the need to rush to the toilet and so gives people more warning and more time to find a toilet before they leak. TPTNS also increases the volume of urine the bladder is able to hold, so people do not need to empty their bladder as often. TPTNS has been tested in ten small studies but only one involved older people living in care homes and it only included 30 people. So far the studies have all indicated that TPTNS is safe and acceptable and that it can help bladder problems. However better quality evidence is needed that it works before it can be recommended for use in everyday treatment. In this research the investigators will test TPTNS compared to dummy treatment in 500 people living in care homes who have urinary incontinence and who wear absorbent pads. The amount of urine they leak into participants' pads will be measured over a 24 hour period after six weeks (at the end of the TPTNS treatment programme) and after three and five months. This will tell the investigators if the treatment works and if it decreases leakage and if so, for how long. The investigators will ask the older person whether they feel their bladder leakage has changed and about any impact on their quality of life. The opinions of close family members and care home staff will be sought regarding whether they think TPTNS has had any effect on the participant. The investigators are also interested to learn about experiences of TPTNS, from residents, family and friends and all the staff involved. Costs of providing this treatment compared to the costs of providing continence care and pads will be determined and. the best ways to give TPTNS treatment in a care home, long term, will be explored with the care home staff.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A pragmatic, multicentre, placebo controlled randomised parallel group trial
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Participants & primary researchers will be blinded to group allocation
Allocation
Randomized
Enrollment
408 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TPTNS Intervention
Arm Type
Experimental
Arm Description
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.
Arm Title
Sham stimulation
Arm Type
Sham Comparator
Arm Description
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.
Intervention Type
Device
Intervention Name(s)
Transcutaneous posterior tibial nerve stimulation
Intervention Description
12 session programme (a total of 6 hours) is delivered in 30 minute sessions twice weekly over a 6 week period of tibial nerve stimulation
Intervention Type
Device
Intervention Name(s)
Sham stimulation
Intervention Description
12 session programme (a total of 6 hours) is delivered in 30 minute sessions twice weekly over a 6 week period of of the lateral sub-malleolar area
Primary Outcome Measure Information:
Title
Volume of UI leaked
Description
Volume of UI leaked over a 24 hour period
Time Frame
6 weeks post randomisation.
Secondary Outcome Measure Information:
Title
Pad use
Description
Number of pads used in 24 hours
Time Frame
6, 12 and 18 weeks post randomisation
Title
PVRU volume
Description
Post-void residual volume of urine scanned in bladder
Time Frame
6, 12 and 18 weeks post randomisation
Title
PBBC
Description
Patient Perception of Bladder Condition
Time Frame
6, 12 and 18 weeks post randomisation
Title
FC-PBC
Description
Family Carer Perception of Bladder Condition
Time Frame
6, 12 and 18 weeks post randomisation
Title
S-PBC
Description
Staff Perception of Bladder Condition
Time Frame
6, 12 and 18 weeks post randomisation
Title
Resident DEMQOL
Description
Resident perception of quality of life
Time Frame
6 and 18 weeks post randomisation
Title
Staff DEMQOL
Description
Staff perception of quality of life
Time Frame
6 and 18 weeks post randomisation
Title
RUQ
Description
Economic evaluation via a resource use questionnaire
Time Frame
6 and 18 weeks post randomisation.
Title
Semi structured interviews with residents, carers and staff regarding the impact of experiences of the TPTNS intervention and any impact on quality of life
Description
Exploration of the experiences of the TPTNS intervention from the perspectives of residents, family carers and care home staff.
Time Frame
6 and 12 weeks post randomisation
Title
Semi-structured interviews and focus groups with care home staff and managers regarding the potential for integrating TPTNS into routine care within care homes, long-term
Description
Exploration of the factors affecting intervention implementation in the care home context and optimisation for sustainability
Time Frame
6-24 weeks post randomisation

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joanne Booth, Prof
Organizational Affiliation
Glasgow Caledonian University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Glasgow Caledonian University
City
Glasgow
ZIP/Postal Code
G4 0BA
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
23206722
Citation
Booth J, Hagen S, McClurg D, Norton C, MacInnes C, Collins B, Donaldson C, Tolson D. A feasibility study of transcutaneous posterior tibial nerve stimulation for bladder and bowel dysfunction in elderly adults in residential care. J Am Med Dir Assoc. 2013 Apr;14(4):270-4. doi: 10.1016/j.jamda.2012.10.021. Epub 2012 Nov 30.
Results Reference
background
PubMed Identifier
34167637
Citation
Booth J, Aucott L, Cotton S, Davis B, Fenocchi L, Goodman C, Hagen S, Harari D, Lawrence M, Lowndes A, Macaulay L, MacLennan G, Mason H, McClurg D, Norrie J, Norton C, O'Dolan C, Skelton D, Surr C, Treweek S. Tibial nerve stimulation compared with sham to reduce incontinence in care home residents: ELECTRIC RCT. Health Technol Assess. 2021 Jun;25(41):1-110. doi: 10.3310/hta25410.
Results Reference
derived
PubMed Identifier
31843002
Citation
Booth J, Aucott L, Cotton S, Goodman C, Hagen S, Harari D, Lawrence M, Lowndes A, Macaulay L, MacLennan G, Mason H, McClurg D, Norrie J, Norton C, O'Dolan C, Skelton DA, Surr C, Treweek S. ELECtric Tibial nerve stimulation to Reduce Incontinence in Care homes: protocol for the ELECTRIC randomised trial. Trials. 2019 Dec 16;20(1):723. doi: 10.1186/s13063-019-3723-7.
Results Reference
derived

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ELECtric Tibial Nerve Stimulation to Reduce Incontinence in Care Homes

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