Urinary Incontinence. Other specified urinary incontinence
Conditions
Interventions
Intervention 1: Intervention group: The patients in group 1 will receive therapy with TENS (model EN-Stim 4
ENRAF-NONIUS Company Ltd, Rotterdam, the Netherlands) for 30 mins once daily for 4 weeks in the hospital (as inpatients or outpatients). The TENS device will use a four-channel stimulator with fully i
Sponsors
Khyber Medical University, Peshawar
Eligibility
Sex/Gender
All
Age
No minimum to 60 Years
Inclusion criteria
Inclusion criteria: Patients with UI after stroke Patients who were stable, cooperative, and could effectively communicate (to participate in therapy Patients who could complete the survey on urination both before and after treatment
Exclusion criteria
Exclusion criteria: Patients with urinary retention Patients with a history of UI for various reasons (Parkinson’s disease, spinal cord disease, dementia, urinary tract tumours, urolithiasis, unhealed urinary tract infections, or a history of urinary tract surgery) Patients who needed significant fluid infusions or drugs that affected urination Patients with concurrent serious organic diseases Patients with severe cognitive functioning disorders (Mini-Mental State Examination10 score <22 points)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overactive Bladder Symptom Score (OABSS). Timepoint: Pre intervention and after 4 weeks of intervention. Method of measurement: Questionnaire. | — |
Countries
Pakistan
Contacts
Public ContactMujeeb Ur Rahman
Khyber Medical University, Peshawar
Outcome results
None listed