The Effect of Occupational Therapy Self-Management Intervention on Expected Outcomes in People with Non-Specific Chronic Low Back Pain

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220520054924N1

Enrollment

Registered

2022-06-18

Start date

2022-12-22

Completion date

Unknown

Last updated

2022-06-27

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

Conditions

Non-Specific Chronic Low Back Pain. Low back pain

Interventions

Intervention 1: Intervention group- Occupational therapy self-management program with stability exercises: In addition to receiving stability exercises (similar to the control group), the intervention

Eligibility

Sex/Gender

All

Age

30 Years to 60 Years

Inclusion criteria

Inclusion criteria: 30-60 years of age At least 12 weeks (3 months) of unilateral or bilateral low back pain at the time of invitation to participate in the study No history of trauma or surgery in the lumbar region during the past year Pain intensity of 3-7 based on visual analog scale Not receiving new rehabilitation or medicine services during the last three months No disc herniation or signs of pressure on the nerve root

Exclusion criteria

Exclusion criteria: Unwillingness or inability to continue their participation in the program An absence of more than three alternating sessions or two consecutive sessions in the program Participation in another rehabilitation program or receiving new medication services related to low back pain

Design outcomes

Primary

Measure	Time frame
Satisfaction with performance in daily living activities. Timepoint: Before the first intervention session, After the last intervention session, One month after the last intervention session. Method of measurement: Canadian Occupational Performance Measure.	—

Secondary

Measure	Time frame
Pain intensity. Timepoint: Before the first intervention session, After the last intervention session, One month after the last intervention session. Method of measurement: Visual Analogue Scale (VAS).;Disability. Timepoint: Before the first intervention session, After the last intervention session, One month after the last intervention session. Method of measurement: Roland Morris Questionnaire.;Performance in daily living activities. Timepoint: Before the first intervention session, After the last intervention session, One month after the last intervention session. Method of measurement: Canadian Occupational Performance Measure.;Fear of movement. Timepoint: Before the first intervention session, After the last intervention session, One month after the last intervention session. Method of measurement: Tampa scale for kinesio-phobia.	—

Measure

Time frame

Pain intensity. Timepoint: Before the first intervention session, After the last intervention session, One month after the last intervention session. Method of measurement: Visual Analogue Scale (VAS).;Disability. Timepoint: Before the first intervention session, After the last intervention session, One month after the last intervention session. Method of measurement: Roland Morris Questionnaire.;Performance in daily living activities. Timepoint: Before the first intervention session, After the last intervention session, One month after the last intervention session. Method of measurement: Canadian Occupational Performance Measure.;Fear of movement. Timepoint: Before the first intervention session, After the last intervention session, One month after the last intervention session. Method of measurement: Tampa scale for kinesio-phobia.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Maryam Binesh

Semnan University of Medical Sciences

maryam.binesh@semums.ac.ir+98 23 3365 4180

Outcome results

None listed

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