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The effect of Biodex Balance System on Degenerative Spondylolisthesis

The effect of adding training on Biodex Balance system to stabilization exercise on pain and function of patients with low back pain from degenerative spondylolisthesis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015111121139N2
Enrollment
30
Registered
2017-01-01
Start date
2016-01-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Degenerative Spondylolisthesis. Spondylolisthesis

Interventions

Intervention 1: Control group will receive conventional TENS (frequency 100 hz and pulse duration 100 micro second) for 30 minutes on the pain area in low back. In addition strengthening, stretching
Rehabilitation
Control group will receive conventional TENS (frequency 100 hz and pulse duration 100 micro second) for 30 minutes on the pain area in low back. In addition strengthening, stretching and stabilizing
Intervention group will receive conventional TENS (frequency 100 hz and pulse duration 100 micro second) for 30 minutes on the pain area in low back. In addition strengthening, stretching and stabiliz

Sponsors

Vice chancellor for research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1. Patients with low back pain whose pain has been related to degenerative spondylolisthesis; Age between 30 and 70; BMI :18.5-30;No history of fracture or surgery in the vertebral column; Not having obvious mental and psychological problems; Have not received physiotherapy treatment during last 6 months Exclusion criteria: using anti pain medicine during treatment; If patient disagrees to continue treatment; patient not comply with exercise regimen at home

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Functional disability. Timepoint: Baseline, after 10 treatment sessions, after 2 months followup. Method of measurement: Functional Rating Index questionnaire.;Pain. Timepoint: Baseline- after 10 treatment sessions- after 2 months followup. Method of measurement: Visuall Analougue Scale.

Secondary

MeasureTime frame
Postural Stability Index. Timepoint: At baseline-After 10 sessions treatment- After 2 months followup. Method of measurement: Overall stability index given by Biodex software during postural test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Safoora Ebadi

Iran University of Medical sciences, Faculty of Medicine

ebadi.s@iums.ac.ir; e_safoora@hotmail.com+98 21 8214 1229

Outcome results

None listed

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