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pain education for Marathi population having persistent low back pain.

A process evaluation of culturally appropriate pain science education for Marathi-speaking people with chronic low back pain - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056003
Enrollment
197
Registered
2023-08-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: M255- Pain in joint

Interventions

Intervention1: Pain science education: Patients assigned to this group will also be given same protocolas control group
additional experimental group will receive a Pain science educationconsistingofonehoursessionwithafrequencyofthreesessionsperweek.Theintervention will be given for two weeks. Total six sessions of PSE

Sponsors

MGM Rehabilitation and fitness centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Marathi speaking individual with CLBP of both the gender in the age group of 18-65years. 2. Non-specific CLBP of more than 3 months duration having a mean pain frequency of >=3days/week. 3.Not receiving concurrent rehabilitation during the study and willing to participate.

Exclusion criteria

Exclusion criteria: 1. Pregnant women and women up to 12 months postpartum. 2. Any structural impairment, pelvic inflammatory disorder, radicular symptoms, fracture or surgical intervention of the spine in the last year. 3. Patients with an uncontrolled mental health condition (e.g. schizophrenia, bipolar disorder, and major depressive disorder) resulting in a negative effect on successful participation. 4. Patients having specific pathologies, malignancy or cancer-related pain.

Design outcomes

Primary

MeasureTime frame
Primary outcome measures: The primary outcome measures are: pain intensity measuredwith the Numerical Rating of Pain Scale (NRS), perceived disability based on the Roland-MorrisDisability Questionnaire(RMDQ)and qualityof life(QoL).Timepoint: All primary outcomes are evaluated at three time points as follows: at baseline (Day 1), after Week 1 and at the end of one-month follow-up (Week4).

Secondary

MeasureTime frame
Secondary outcome measures: Revised Neurophysiology of Pain Questionnaire (r-NPQ), Pain Beliefs Questionnaire(PBQ), Tampa scale of KinesiophobiaTimepoint: All secondary outcomes are evaluated at three time points as follows: at baseline (Day 1), after Week 1 & at the end of one-month follow-up (Week4).

Countries

India

Contacts

Public ContactRinkle Hotwani

MGM School of Physiotherapy

tabishfahim4u@gmail.com08368148230

Outcome results

None listed

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