Effects of a combined exercise intervention program with cognitive physical therapy on women with chronic non-specific low back pain

Effects of a combined exercise intervention program with cognitive physical therapy on pain, disability and postural sway on women with chronic non-specific low back pain

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220722055522N1

Enrollment

Registered

2022-12-03

Start date

2022-12-11

Completion date

Unknown

Last updated

2023-02-07

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

Conditions

Low Back Pain. Low back pain

Interventions

Intervention 1: Intervention group 1: Performing combined exercises that include eight weeks of aerobic, endurance, strength, and flexibility exercises. Intervention 2: Intervention group 2: Conductin

Eligibility

Sex/Gender

Female

Age

20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Suffering from non-specific chronic back pain (with a history of pain for at least 3 months) Absence of cardiorespiratory diseases Absence of neuromuscular diseases Not having diabetes No history of surgery No history of fracture Not having a history of serious injuries in the spine, including disc herniation Not having obvious structural abnormalities in the spine No difference in leg length Obtaining a disability score equal to or greater than 4 in the Roland Morris Disability Questionnaire Obtaining a score of at least 3 from the visual pain measurement scale

Exclusion criteria

Exclusion criteria: Having neuropathic pain, history of previous lumbar spine surgery history of previous lumbar spine surgery Mental disability Severe mental illness Illiteracy If the subjects do not regularly participate in the training sessions (two consecutive sessions and three non-consecutive sessions), they will be excluded from the study.

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: Before and after intervention. Method of measurement: The visual analogue scale.;Disability. Timepoint: Before and after intervention. Method of measurement: The roland-morris disability questionnaire.	—

Secondary

Measure	Time frame
Postural sway. Timepoint: Before and after intervention. Method of measurement: Foor scan.;Quality of life. Timepoint: Before and after intervention. Method of measurement: SF-36questionnaire.;Kinesiophobia. Timepoint: Before and after intervention. Method of measurement: Kinesiophobia questionnaire.;The balance. Timepoint: Before and after intervention. Method of measurement: Y balance test.;Walking. Timepoint: Before and after intervention. Method of measurement: Foot scan.;Muscular endurance. Timepoint: Before and after intervention. Method of measurement: Sorensen's test.	—

Measure

Time frame

Postural sway. Timepoint: Before and after intervention. Method of measurement: Foor scan.;Quality of life. Timepoint: Before and after intervention. Method of measurement: SF-36questionnaire.;Kinesiophobia. Timepoint: Before and after intervention. Method of measurement: Kinesiophobia questionnaire.;The balance. Timepoint: Before and after intervention. Method of measurement: Y balance test.;Walking. Timepoint: Before and after intervention. Method of measurement: Foot scan.;Muscular endurance. Timepoint: Before and after intervention. Method of measurement: Sorensen's test.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Raeisi

Arak University

Z_raisi13@yahoo.com+98 86 3417 3492

Outcome results

None listed

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