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Effect of Graded Sensory and Motor Retraining on pain, fear of movement and posture in young adults population with non-specific chronic low back pain.

Effect of Graded Sensorimotor Retraining on pain, kinesophobia and postural stability among young adults with non-specific chronic low back pain: A Randomised Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/068081
Enrollment
56
Registered
2024-05-30
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

hold up to 5seconds. Progresses up to 10 repetitions
hold up to 10 seconds.
Intervention1: Sensorimotor Retraining: Participants included in this group will be given graded sensorimotor retraining which includes treatment divided in 8stages which is categorized in two segme
all the 3 days treatment will be given by considering both aspects i.e. both sensory retraining and motor retraining. Control Intervention1: Conventional Physical therapy: Conventional Physical therap

Sponsors

Nitte Instituteof Physiotherapy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Students who are 18 to 28 years of age 2)Both male & female 3)Chronic low back pain of a non-specific nature 4)Young individuals suffering from at least a single episode of back pain in the past 3 months 5)NPRS ( Numerical Pain Rating Scale) score between 3 out of 10 to 8 outof 10

Exclusion criteria

Exclusion criteria: 1)Presence of neurological signs (e.g., perceived weakness in the lower limbs) 2)A diagnosed psychiatric disorder or severe cognitive impairment 3)Having the specific disease (e.g., malignancy, inflammatory joint and bone disease)

Design outcomes

Primary

MeasureTime frame
1) Numerical Pain Rating Scale 2) TAMPA scale for kinesophobia 3) Multidirectional functional reach test Timepoint: Once the individual is included in the study, readings will be taken as baseline values and after 8 weeks of treatment.

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactNityal Kumar Alagingi

Nitte Institute of Physiotherapy NITTE (Deemed to be university)

nityalkumar2020@nitte.edu.in7760547669

Outcome results

None listed

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