A Comprehensive Program for Reducing Chronic Body Pain with Psychotherapy and Rehabilitation

An interdisciplinary pain management program for patients with chronic musculoskeletal pain using psychiatric treatment and rehabilitation

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20250728066663N1

Enrollment

Registered

2025-12-01

Start date

2025-03-21

Completion date

Unknown

Last updated

2025-12-08

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

Conditions

Chronic Musculoskeletal Pain. Chronic pain, not elsewhere classified

Interventions

Intervention 1: Intervention group: Pharmacotherapy with Physiotherapy. Physiotherapy was administered over a six-week period, comprising a total of 8 to 12 treatment sessions delivered twice weekly.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis of chronic musculoskeletal pain Possibility of at least 6 months follow-up Moderate or higher severity of psychiatric disorder Moderate or higher severity of functional disability

Exclusion criteria

Exclusion criteria: Pain duration less than 3 months Pain associated with an underlying disease or a specific trauma Lack of patient cooperation or inability to ensure at least 6 months of follow-up

Design outcomes

Primary

Measure	Time frame
Pain score based on the visual analogue score. Timepoint: Baseline, sixth month follow-up. Method of measurement: Visual analogue score.;Pain score based on the Million visual analogue score. Timepoint: Baseline, sixth month follow-up. Method of measurement: Million visual analogue score.;Disability severity assessment using Oswestry Disability Index. Timepoint: Baseline, sixth month follow-up. Method of measurement: Oswestry Disability Index Questionnaire.	—

Measure

Time frame

Pain score based on the visual analogue score. Timepoint: Baseline, sixth month follow-up. Method of measurement: Visual analogue score.;Pain score based on the Million visual analogue score. Timepoint: Baseline, sixth month follow-up. Method of measurement: Million visual analogue score.;Disability severity assessment using Oswestry Disability Index. Timepoint: Baseline, sixth month follow-up. Method of measurement: Oswestry Disability Index Questionnaire.

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Secondary

Measure	Time frame
Depression score using Beck Questionnaire. Timepoint: Baseline, sixth month follow-up. Method of measurement: Beck Depression Inventory II.;Post-traumatic Stress Disorder score using PCL-M questionnaire. Timepoint: Baseline, sixth month follow-up. Method of measurement: Post-traumatic Stress Disorder (PTSD) checklist-Military (PCL-M).;Quality of Life score based on SF-36. Timepoint: Baseline, sixth month follow-up. Method of measurement: Short Form 36 Health Survey (SF36).;Functional Capacity using PILE Test. Timepoint: Baseline, sixth month follow-up. Method of measurement: Progressive Isoinertial Lifting Evaluation.	—

Measure

Time frame

Depression score using Beck Questionnaire. Timepoint: Baseline, sixth month follow-up. Method of measurement: Beck Depression Inventory II.;Post-traumatic Stress Disorder score using PCL-M questionnaire. Timepoint: Baseline, sixth month follow-up. Method of measurement: Post-traumatic Stress Disorder (PTSD) checklist-Military (PCL-M).;Quality of Life score based on SF-36. Timepoint: Baseline, sixth month follow-up. Method of measurement: Short Form 36 Health Survey (SF36).;Functional Capacity using PILE Test. Timepoint: Baseline, sixth month follow-up. Method of measurement: Progressive Isoinertial Lifting Evaluation.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Ebrahimzadeh Babaki

Iran University of Medical Sciences

amirebrahimzadeh13@gmail.com+98 21 8670 2030

Outcome results

None listed

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