Effects of Transcutaneous Tibial Nerve Stimulation for Overactive Bladder Symptoms in Adults

Sponsor
Dow University of Health Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT05464589
Collaborator
(none)
60
3
2
15.7
20
1.3

Study Details

Study Description

Brief Summary

For overactive bladder symptoms, there are numerous physiotherapy techniques have been found to be beneficial. Transcutaneous electrical stimulation of the tibial nerve is one of those treatment options, that is entirely a non-invasive, easy to apply, and cost-effective technique.

Transcutaneous stimulation of the tibial nerve targets the sacral nerve plexus that contracts the pelvic floor muscles and controls the bladder function.

This research aims to study the effectiveness of transcutaneous tibial nerve stimulation in adults with overactive bladder symptoms along with the conventional physiotherapy for overactive bladder (pelvic floor muscle training through Kegel's exercises) among 60 patients with overactive bladder symptoms on the basis of non-probability purposive sampling technique with screening for study criteria through a consultant urologist. After taking informed consent, all participants will be randomly allocated into two groups. Group A will receive pelvic floor muscles training through Kegels exercises along with transcutaneous electrical stimulation of the tibial nerve and Group B will receive pelvic floor muscles training through Kegels exercises. The treatment duration will of six weeks. Outcomes will be assessed before the start of the treatment and after the end of the treatment sessions.

Condition or Disease Intervention/Treatment Phase
  • Other: Transcutaneous tibial nerve stimulation along with pelvic floor muscle srengthening
  • Other: Pelvic floor muscles strengthening
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
It is a randomized control trial. Total 60 patients will be recruited, 30 in each group. Treatment will be allocated using a random number sheet generated by SPSS software version 21. Participants are assigned to one of two groups in parallel for the duration of the study.It is a randomized control trial. Total 60 patients will be recruited, 30 in each group. Treatment will be allocated using a random number sheet generated by SPSS software version 21. Participants are assigned to one of two groups in parallel for the duration of the study.
Masking:
Single (Outcomes Assessor)
Masking Description:
The outcome accessor involved in the clinical trial will be prevented from having knowledge of the interventions to the individual participants of each group.
Primary Purpose:
Treatment
Official Title:
Effects of Transcutaneous Tibial Nerve Stimulation for Overactive Bladder Symptoms in Adults: A Randomized Control Trial
Actual Study Start Date :
Aug 10, 2021
Anticipated Primary Completion Date :
Oct 30, 2022
Anticipated Study Completion Date :
Nov 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Transcutaneous Tibial Nerve Stimulation + Pelvic Floor Muscle Strengthening

Pelvic floor muscle strengthening through Kegel exercises along with the transcutaneous tibial nerve stimulation. Pelvic Floor Muscle-strengthening exercises - Kegels' exercises 15 repetitions, 3 times a day For 6 weeks, daily. Transcutaneous Tibial Nerve Stimulation for 30 minutes on the right lower limb 6 sessions, one per week.

Other: Transcutaneous tibial nerve stimulation along with pelvic floor muscle srengthening
Pelvic floor muscles strengthening: Pelvic floor muscles training involves Kegel's exercises. Kegel exercises improve the function and tone of the pelvic floor. Kegel exercises represent the voluntary contraction and relaxation of the levator ani muscle (principally the pubococcygeus and puborectalis portions), which supports the vagina, bladder, and urethra. The slow contractions help with muscle strengthening. Transcutaneous electrical stimulation of Tibial Nerve: Transcutaneous Tibial nerve stimulation is a form of treatment technique that involves the use of electrical impulses to address urinary symptoms and target the lower urinary tract.

Active Comparator: Pelvic Floor Muscle Strengthening

Pelvic floor muscle strengthening through Kegel exercises. Pelvic floor muscle exercises - Kegels; exercises 15 repetitions, 3 times a day For 6 weeks, daily.

Other: Pelvic floor muscles strengthening
Pelvic floor muscles strengthening: Pelvic floor muscles training involves Kegel's exercises. Kegel exercises improve the function and tone of the pelvic floor. Kegel exercises represent the voluntary contraction and relaxation of the levator ani muscle (principally the pubococcygeus and puborectalis portions), which supports the vagina, bladder, and urethra. The slow contractions help with muscle strengthening.

Outcome Measures

Primary Outcome Measures

  1. Change in Overactive Bladder Symptom Score from baseline at sixth week [At baseline and after 6 weeks]

    OABSS is a validated instrument which evaluates the four cardinal symptoms (day and nighttime frequency, urgency, and urge incontinence) of OAB in a one score. A total OABSS score of 3 or more and an urgency score of 2 or more is the recommended cut-off for diagnosing OAB, and the severity is further divided into mild (total score of 3-5 points), moderate (6-11 points) and severe (12 or more points). Patients will be evaluated at baseline and 6 weeks after the intervention through OABSS.

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinically diagnosed overactive bladder

  • A total OABSS score of 3 or more and an urgency score of 2 or more

  • 30-65 years old

Exclusion Criteria:
  • Pregnancy

  • Acute urinary tract infection (within 15 days)

  • Any surgical procedure for urinary incontinence

  • Genito-urinary cancer history

  • Stage II pelvic organ prolapse according to pelvic organ prolapse-quantification system

  • Lesion on the site of stimulation or around it

  • Pelvic pacemakers

  • Lower limbs prostheses

  • Patients who will not be able to perform Kegel's exercises

  • An impaired sensation at the site of stimulation.

  • Patients receiving any treatment other than the prescribed medications by the referring physician (that will be the same for all patients of both groups) will be excluded.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dow University Hospital Karachi Sindh Pakistan
2 Dow University of Health Sciences Karachi Sindh Pakistan
3 Sindh Institute of Physical Medicine and Rehabilitation Karachi Sindh Pakistan

Sponsors and Collaborators

  • Dow University of Health Sciences

Investigators

  • Principal Investigator: Sana Subhan, DPT, Dow University of Health Sciences
  • Study Director: Dr. Syed Imran Ahmed, MBBS, FCPS, Sindh Institute of Physical Medicine and Rehabilitation
  • Study Director: Dr. Muhammad Hammad Mithani, MBBS, FCPS, Dow University Hospital
  • Study Director: Aftab Ahmed Mirza Baig, DPT, MSAPT, Sinsh Institute of Physical Medicine and Rehabilitation

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Sana Subhan, Principal Investigator, Dow University of Health Sciences
ClinicalTrials.gov Identifier:
NCT05464589
Other Study ID Numbers:
  • SSubhan
First Posted:
Jul 19, 2022
Last Update Posted:
Jul 19, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sana Subhan, Principal Investigator, Dow University of Health Sciences
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 19, 2022