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Effect of Cognitive Behavioral Therapy in Patients With Chronic Nonspecific Low Back Pain

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Low Back Pain, Mechanical

Treatments

Other: Cognitive Behavioral Therapy
Other: Home program exercises

Study type

Interventional

Funder types

Other

Identifiers

NCT04938739
Manis_MSc

Details and patient eligibility

About

The purpose of the study is to determine the effectiveness of cognitive-behavioral therapy on functional outcomes, pain, and pain-related anxiety in patients with chronic nonspecific low back pain

Full description

Back pain has considerable negative effects on the quality of life of affected individuals. Individuals with new-onset back pain have an increased risk of lower quality of life scores, and the negative effect on quality of life increases with persistent pain. Patients with chronic back pain report a quality of life that is lower than individuals without pain and that is comparable to those of individuals with life-threatening diagnoses. In addition, back pain is associated with worry and fears, particularly about the (sense of) self and socialrelationships and especially when pain persists longer than expected.

Enrollment

30 patients

Sex

All

Ages

20 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Thirty patients with non-specific chronic low back pain from both sexes will be included.
  2. Subjects with normal body mass index (18 to 25).
  3. The age of patients range from 20 to 35 years.
  4. Duration of pain more than 3 months up to 2 years.
  5. Normal cognition score 26 or above according to MoCA Scale.7. Highly educated at least high school.

Exclusion criteria

The patients will be excluded if they have any of the followings:

  1. Lumbar canal stenosis.
  2. Lumbar discogenic lesions.
  3. Any inflammatory arthritis, tumors, infection involving the lumbar spine.
  4. Patients with decreased range of motion secondary to congenital anomalies, muscular contracture or bony block.
  5. Previous lumbar surgery or trauma.
  6. Subjects with a history of any neurologic disease.
  7. Cauda equina Syndrome.
  8. Patients suffering from psychological, cognitive or emotional disturbance.
  9. Patients who had previously participated in cognitive behavioral therapy.
  10. Deafness and blindness.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Cognitive Behavioral therapy
Experimental group
Description:
to modify any erroneous beliefs about pain and disability and to promote coping strategies and self-efficacy through a graded activity.
Treatment:
Other: Home program exercises
Other: Cognitive Behavioral Therapy
Home program exercises
Active Comparator group
Description:
Patients in both groups carried out exercise therapy for six weeks. There will be an educational session for each patient to make sure the exercises will be done successfully and supervision once per week.
Treatment:
Other: Home program exercises

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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