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Effect of Virtually administered Physiotherapy Vs In person physiotherapy for Chronic non specific low back pain in young adults.

Efficacy of a virtually administered physiotherapy program in chronic non-specific low back pain in young adults. A single blinded randomised controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/10/037168
Enrollment
98
Registered
2021-10-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: M708- Other soft tissue disorders related to use, overuse and pressure

Interventions

Intervention1: Low back exercise program: back strengthening exercises, Stretching exercises, Core exercises, Ergonomics, Postural re education Intervention2: Low back exercise programme administered

Sponsors

Priti Mehendale
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Males and females in the age group of 20-40 years suffering from chronic non specific low back pain and willing to participate in the study

Exclusion criteria

Exclusion criteria: Individuals with chronic low back pain with a neural component, i.e., diagnosed and /or presenting with a prolapsed intervertebral disc and/or radiculopathy. Individuals with congenital/traumatic/infective/inflammatory affections of the spine, upper limb/s and lower limb/s. Individuals with chronic low back pain having recently undergone a surgery of the spine and / or lower limb/s and/or upper limb/s. Individuals with a pain intensity =7 on NPRS. Individuals suffering from severe cardiovascular disease and/or metabolic, autoimmune disease. Individuals with a BMI of = 30 kg/m2 Individuals suffering from any neurological disorder. Pregnant females. Individuals diagnosed with osteoporosis. Individuals on a graded exercise programme

Design outcomes

Primary

MeasureTime frame
Numerical Pain Rating Scale (NPRS), Modified modified Schobers test (MMST), Roland Morris Disability Questionnaire(RMDQ 24),World Health Organization Quality of Life BREF (WHO QOL BREF),Tampa Scale of Kinesiophobia (TSK-11), Patient Satisfaction Questionnaire (PSQ 18) Timepoint: 0 3 5 weeks—

Secondary

MeasureTime frame
Tampa Scale of Kinesiophobia (TSK18), Patient Satisfaction Questionnaire (PSQ 18)Timepoint: 0 3 5 weeks—

Countries

India

Contacts

Public ContactPriti Mehendale

Parul University

madhavan.iyenagar77544@paruluniversity.ac.in9324707024

Outcome results

None listed

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