Effects of Transcutaneous Electrical Nerve Stimulation with Home-Based Program in Postpartum Patients with Low Back Pai
Not Applicable
Recruiting
- Conditions
- ow Back Pain.Low Back PainM54.5
- Registration Number
- IRCT20210205050256N2
- Lead Sponsor
- niversity of Lahore
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Age range between 18 to 40 years
Female who have normal delivery
Female with six week post-partum
Female having low back pain
Exclusion Criteria
Anatomical anomaly
Structural disorder of spinal alignment (Scoliosis, kyphosis, lordosis)
Traumatic / Inflammatory / Infectious Conditions
Diagnosed stress / depression / Anxiety
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Numeric Pain Rating Scale (NPRS).;Disability. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Modified Oswestry Disability Index (MODI).;Quality of Life. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Short-Form 36.
- Secondary Outcome Measures
Name Time Method