effect of neuromuscular training on core stability, proprioception and pain in women with chronic low back pain

Comparison of the effect of 8 weeks of supervised and home based neuromuscular training on core stability, proprioception and pain in house wives with chronic low back pain

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200107046035N2

Enrollment

Registered

2020-05-26

Start date

2020-05-20

Completion date

Unknown

Last updated

2020-06-15

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: supervised neuromuscular training at home for 8 weeks, 3 sessions per week, 1 hour per session. Intervention 2: Intervention group: home-based neuromuscular trainin

Eligibility

Sex/Gender

Female

Age

30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Female gender age between 30-60 years No specific disease Do not use other therapies

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Low back pain. Timepoint: At the beginning of the study (before the start of the intervention) and after 8 weeks of intervention. Method of measurement: VAS scale.;Trunk control defects. Timepoint: At the beginning of the study (before the start of the intervention) and after 8 weeks of intervention. Method of measurement: McGill and Berens-Sorensen test, goniometer.;Central body disorders. Timepoint: At the beginning of the study (before the start of the intervention) and after 8 weeks of intervention. Method of measurement: McGill and Berens-Sorensen test, goniometer.	—

Measure

Time frame

Low back pain. Timepoint: At the beginning of the study (before the start of the intervention) and after 8 weeks of intervention. Method of measurement: VAS scale.;Trunk control defects. Timepoint: At the beginning of the study (before the start of the intervention) and after 8 weeks of intervention. Method of measurement: McGill and Berens-Sorensen test, goniometer.;Central body disorders. Timepoint: At the beginning of the study (before the start of the intervention) and after 8 weeks of intervention. Method of measurement: McGill and Berens-Sorensen test, goniometer.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Shahrokhi

Hakin Sabzevari University

h.shahrokhi@hsu.ac.ai+98514401101

Outcome results

None listed

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