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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 Pain
M54.5
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
NameTimeMethod
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
NameTimeMethod
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