Effect of Tibial Transcutaneous Electrostimulation in Women With Urgency Urinary Incontinence

Urinary Incontinence, Urge Clinical Trial

— TibialTNS  

Official title:

Effect of Tibial Transcutaneous Electrostimulation in Women With Urgency Urinary Incontinence Compared to a Sham Group: Randomized Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05590481
• Other study ID #: TIBIALTENS
• Status: Recruiting
• Phase: N/A
• Start date: January 23, 2023
• Est. completion date: December 30, 2023

Study information

• Verified date: February 2023
• Source: Instituto Materno Infantil Prof. Fernando Figueira
• Contact: Priscila Bezerra, MS
• Phone: +5581988571614
• Email: priscilabezerra1382[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Urge urinary incontinence (UUI) is associated with nocturia, a common cause of sleep disorders, also related to levels of anxiety and depression. Studies demonstrate improvement in the clinical parameters of women with UUI after treatment with transcutaneous tibial nerve stimulation (TTNS). However, there are few data available on the association of urinary symptoms in women with UUI with sedentary behavior (SB), physical activity level (PAL) and sleep quality (SQ). Our study has the objective of evaluating the impact of TTNS on urinary symptoms, anxiety level, life quality(LQ), sleep parameters, PAL and SB in women with UUI.

Description:

A randomized clinical trial, sham-controlled, comparing behavioral therapy and TTNS (intervention) to the use of behavioral therapy alone. It will include women with 18 years or more, diagnosed with UUI or mixed IU attested by the Questionnaire Overactive Bladder Validated 8 (OAB-V8).

Women with active urinary tract infection in the last four weeks, alcoholics, smokers or drug addicts, with lesions and alteration of skin sensitivity in the place where electrotherapy will be applied, in drug and/or physiotherapeutic treatment for UUI or current OAB, using sleep-inducing medication, with any neurological disease, using anticholinergic drugs, calcium antagonists, antagonists and dopamine antagonists, with presence of pelvic organ prolapse, during pregnancy or puerperal or with any difficulty in understanding or cognitive deficit that makes it impossible to carry out the research will be excluded.

Study variables are behavioral therapy, bilateral transcutaneous tibial nerve stimulation, type of UI, PAL, excessive daytime sleepiness, generic and specific LQ, SQ, UI severity, anxiety level, urinary frequency, nocturia and bladder capacity.

Sample size was calculated, adopting a two-tailed test with the following parameters: α = 0.05, β = 0.20 and statistical power of 80% and 102 women will be included.

The study will be carried out in two physiotherapy clinics in Recife, from September 2022 to June 2023, both groups will undergo a behavioral therapy protocol, (bladder training, pelvic floor muscle training and modification of liquid intake). Patients will be submitted to biphasic current and surface electrodes during 12 treatment sessions, twice a week, on non-consecutive days, with a electrical stimulation device (Quark, Brazil). The following parameters will be used for TTNS: frequency 10Hz (dez Hertz), pulse duration 200 μs (microseconds), for 30 minutes. In the experimental group, the electrodes will be positioned on the medial malleolus of both legs), in order to stimulate the tibial nerve path. In the Sham group, the electrodes will be placed on both legs, centered in the middle of the thigh, where there is no stimulus for the tibial or sacral nerve, for 30 minutes.

The project was approved by the Research Ethics Committee of Professor Fernando Figueira Institute of Integral Medicine.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 102
• Est. completion date: December 30, 2023
• Est. primary completion date: July 30, 2023
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Female sex;

• Age from 18 years old;

• Diagnosis of urgency urinary incontinence or mixed urinary incontinence

• Score greater than or equal to 8 on the Hyperactive Bladder - Validated 8 Question Awareness Tool (OAB-V8)

Exclusion Criteria:

• -Active urinary infection in the last four weeks;

• Alcoholism, smoking or drug addiction;

• Lesions and alteration of skin sensitivity in the place where electrotherapy will be applied;

• Drug and/or physiotherapeutic treatment for urgency urinary incontinence;

• Use of sleep-inducing medication,

• Any neurological disease (multiple sclerosis, Alzheimer's disease, stroke and Parkinson's disease);

• Use of anticholinergic drugs, calcium antagonists, b-antagonists and dopamine antagonists;

• Presence of pelvic organ prolapse (POP), measured by a score greater than III by the POP-Q system;

• Any comprehension difficulty or cognitive deficit that makes it impossible to carry out the research;

• Gestational or puerperal period.

Related Conditions & MeSH terms

• Enuresis
• Urinary Incontinence
• Urinary Incontinence, Urge

Intervention

Device:
• TIBIAL TRANSCUTANEOUS ELECTROSTIMULATION
The electrodes will be surface (silicone rubber and carbonate), brand Quark®, with dimensions of 5 cm by 3 cm, coupled with conductive gel and fixed to the volunteer's skin with micropore tape. For the placement of the electrodes, the volunteer will be positioned in the horizontal supine position on the stretcher, with the knee in semiflexion and the head supported on a pillow. The electrodes will be positioned one immediately posterior to the medial malleolus of the ankle and the other approximately 10 cm above it, both fixed with micropore tape, on both legs of the patient. To ensure that the electrodes stimulate the tibial nerve, a transcutaneous electrical nerve stimulation (TENS) current with a frequency of 1 Hz will first be applied, with a gradual increase in intensity, to verify a rhythmic movement of flexion of the hallux. The following parameters will be used for TTNS: frequency 10Hz (Hertz), pulse duration 200 µs (microseconds), for 30 minutes.

Behavioral:
• behavioral therapy protocol
submitted to a behavioral therapy protocol, which involves bladder training, pelvic floor muscle training and modification of liquid intake. The orientation will be based on the initial evaluation of the patient, in which the responsible researcher will give verbal orientations and deliver booklets on the pathology, behavioral therapy and sleep hygiene.

Locations

Country	Name	City	State
Brazil	Instituto de medicina integral fernando figueira	Recife	PE

Sponsors (2)

Lead Sponsor	Collaborator
Instituto Materno Infantil Prof. Fernando Figueira	Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Nocturia	People with an overactive bladder can experience nocturia, which means they need to get up frequently at night to go to the bathroom. Nocturia will be evaluated through the voiding diary that the volunteers will be instructed to complete. The more times the volunteer gets up at night to urinate, the more severe the condition.	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	sleep quality	Assessed by the Pittsburgh Sleep Quality Index (PSQI), with the global score ranging from 0 to 21. The higher, the worse the sleep quality.	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	physical activity level	lifestyle based on the daily number of steps	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	sedentary behavior	lifestyle based on the daily number of steps	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	anxiety level	A mental health disorder characterized by feelings of worry, anxiety, or fear that are strong enough to interfere with daily activities. Screening for study anxiety will be performed using the the Hospital Anxiety and Depression Scale (HADS). The scale is validated for Portuguese and was developed to identify possible cases of anxiety and depression through a structured and easy-to-apply questionnaire.The HADS consists of two subscales of 14 varied questions: 7 questions that measure anxiety (HADS-A) and 7 that measure depression (HADS-D). Each question has four possible answers and a score from 0 to 3 is given. The total score is then calculated and can range between 0 and 21 points on each subscale, with a higher score indicating more severe symptoms. The cut-off score for "possible cases" of anxiety and depression is 8 points or higher, which is the cut-off identified to provide the optimal balance between specificity and sensitivity.	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	Sleep parameters - Total time of sleep	Total time the individual spent sleeping during the night	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	Excessive daytime sleepiness	discrete quantitative variable, assessed using the Epworth sleepiness scale 1 ( ) yes, 2 ( ) no. It is a self-administered questionnaire and refers to the possibility of napping in eight everyday situations.	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	Severity of urinary incontinence	To identify how much the urinary incontinence impacts one's life.The severity of UI will be assessed using the Incontinence Severity Index (ISI), translated and validated into Portuguese by Pereira et al, in 2011 (Appendix 1)(126). This instrument consists of two questions regarding the frequency (1-4 points) and amount (1-3 points) of urinary loss. To obtain the final score, the scores for frequency of urinary leakage and the amount of urinary leakage are multiplied.	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	Life's quality	The SF-36 Medical Outcomes Study 36 - Item Short - Form Health Survey (SF36) is a generic instrument for assessing quality of life that is easy to administer and understand. It consists of a multidimensional questionnaire, consisting of 36 items, encompassed in 8 scales or domains. It has a final score from 0 to 100 (obtained by calculating the Raw Scale), where 0 corresponds to the worst general health status and 100 corresponds to the best health status.	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	Sleep parameters - sleep efficiency	Sleep efficiency is the relationship between the time the patient spent in bed and the actual sleep time.	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	Sleep parameters - Total time in bed	Total time in bed, whether sleeping or not.	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	Sleep parameters - Nightly awakenings	Number of times the individual wakes up during the night	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).
Secondary	Sleep parameters - Time awake after falling asleep	Time awake after sleep started, total time of nocturnal awakenings.	Baseline/ change after the 6th week of treatment /change 30 days after the 6th week of treatment(follow up).