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Evaluation of the effect of lumbopelvic fascial release alone with lumbopelvic and cervical fascial release on pain intensity, functional disability, pressure pain threshold, quality of life and sonoelastography indices of the fascia in both regions in non-specific chronic low back pain patients associated with neck pain

Evaluation of the effect of lumbopelvic fascial release alone with lumbopelvic and cervical fascial release on pain intensity, functional disability, pressure pain threshold, quality of life and sonoelastography indices of the fascia in both regions in non-specific chronic low back pain patients associated with neck pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230502058059N1
Enrollment
44
Registered
2023-07-09
Start date
2023-07-15
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Condition 1: Low back pain. Condition 2: Neck pain. XIII Diseases of the musculoskeletal system and connective tissue XIII Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention 1: The first intervention group: they receive lumbo-pelvic fascial release. Intervention 2: The second intervention group: they receive lumbo-pelvic and cervical fascial release.

Sponsors

University of social welfare and rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: People with the simultaneous complication of non-specific chronic low back pain and neck pain, where the intensity of low back pain is greater compared to the neck pain Age between 20 and 55 years Not having low back pain and neck pain caused by specific pathologies Not receiving painkillers and anti-inflammatory drugs in the last 3-7 days Not currently receiving physical therapy or other treatment

Exclusion criteria

Exclusion criteria: pregnancy Not attending regular therapy sessions Unwillingness to continue participating in the study Infecting or developing cases (after the start of the study) that violates the criteria for entering the study for any reason

Design outcomes

Primary

MeasureTime frame
Pain score on Visual Analog Scale. Timepoint: Before the start of the intervention, at the end of the intervention and after the two-week follow-up. Method of measurement: Visual Analog Scale.;Back disability score in back disability questionnaire. Timepoint: Before the start of the intervention, at the end of the intervention and after the two-week follow-up. Method of measurement: Oswestry Disability Index.;Neck disability score in neck disability questionnaire. Timepoint: Before the start of the intervention, at the end of the intervention and after the two-week follow-up. Method of measurement: Neck Disability Index.

Secondary

MeasureTime frame
Pressure pain threshold score. Timepoint: Before the start of the intervention, at the end of the intervention and after the two-week follow-up. Method of measurement: Algometer tool.;Quality of life score. Timepoint: Before the start of the intervention, at the end of the intervention and after the two-week follow-up. Method of measurement: Short form health survay.;Fascia elasticity. Timepoint: Before the start of the intervention, at the end of the intervention and after the two-week follow-up. Method of measurement: Sonoelastography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoodeh Zandi

University of social welfare and rehabilitation sciences

soodeh.zandi@ymail.com+98 21 2200 6911

Outcome results

None listed

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