Revulsive compress on pain and daily routine among adult low back pain patients

Effect of revulsive compress on pain and activities of daily living among adult lumbago patients- A randomized controlled trial. - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/11/059893

Enrollment

Registered

2023-11-15

Start date

Unknown

Completion date

Unknown

Last updated

2023-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M545- Low back pain

Interventions

Intervention1: Revulsive compress: The study group will undergo revulsive compress to lower back in prone lying position. This involves with alternate application of hot fomentation (98-104 ? F / 36-4

Eligibility

Inclusion criteria

Inclusion criteria: Subjects are age group of = 20 years to = 50 years and both male and female diagnosed with lumbago. History of low back pain not more than 2 years Patients who are able to differentiate sensation of heat and cold.Patients who are able to read or write or understand Tamil or English. Patients who are willing to participate in the study.

Exclusion criteria

Exclusion criteria: Patients with structural spinal deformity. Patients with specific spinal pathology of infection, tumor, fracture, ankylosing spondylitis, osteoporosis, lumbar spondylosis, acute intervertebral disc bulge with radicular syndrome.Women during menstrual bleeding and pregnancy. Patients with recent surgical history and undergone surgery in spine. Patients with renal calculi, pelvic inflammatory disease, acute gastritis, colitis.Patients under anti-spasmodics, anti-cholinergics and steroid medication.

Design outcomes

Primary

Measure	Time frame
Assessment of low back pain and activities of daily living will be measured using Numeric Rating Scale (NRS) and Oswestry Disability Index (ODI) 2.1a -Tamil Questionnaire before and after the 14 days of intervention.Timepoint: Assessment of low back pain and activities of daily living will be measured using Numeric Rating Scale (NRS) and Oswestry Disability Index (ODI) 2.1a -Tamil Questionnaire by 1st and 14th day of intervention.	—

Measure

Time frame

Assessment of low back pain and activities of daily living will be measured using Numeric Rating Scale (NRS) and Oswestry Disability Index (ODI) 2.1a -Tamil Questionnaire before and after the 14 days of intervention.Timepoint: Assessment of low back pain and activities of daily living will be measured using Numeric Rating Scale (NRS) and Oswestry Disability Index (ODI) 2.1a -Tamil Questionnaire by 1st and 14th day of intervention.

—

Secondary

Measure	Time frame
Assessment of spinal flexibility will be measured using Toe-Touch Test (TTT) before and after the 14 days of intervention. Assessment of blood pressure will be taken on before and after 14 days of interventionTimepoint: Assessment of spinal flexibility will be measured using Toe-Touch Test (TTT) and blood pressure will be taken on first and fourteen day of intervention	—

Countries

India

Contacts

Public ContactDr MTamil Selvii

International Institute of Yoga and Naturopathy Medical Sciences, Chengalpattu

drpandiarajamuthupandimd@gmail.com9952448729

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026