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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01323127
Other study ID # LOCAL/2010/AD-03
Secondary ID 2010-A01536-33
Status Completed
Phase N/A
First received March 24, 2011
Last updated March 25, 2015
Start date April 2011
Est. completion date December 2011

Study information

Verified date March 2015
Source Centre Hospitalier Universitaire de Nimes
Contact n/a
Is FDA regulated No
Health authority France: Committee for the Protection of PersonnesFrance: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Observational

Clinical Trial Summary

The main objective of this study is to investigate the influence of seat type (straight chair versus "ergonomic" chair) on the sagittal alignment of the lumbo-pelvic complex in two different postures compared to standing for each individual in both a chronic-back-pain and a non-chronic-back-pain population.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility General Inclusion Criteria:

- The patient must have given his/her informed and signed consent

- The patient must be insured or beneficiary of a health insurance plan

Inclusion Criteria for the Chronic Back Pain Group

- Patient has chronic lombalgia (> 3 months)

- Patient has discopathy evidenced by standard imaging of the lumbar spine

Inclusion Criteria for the Non Chronic Back Pain Group

- Patient does not have chronic lombalgia or neurological symptoms

- Patients hospitalized for cardiovascular physical therapy which does not interfere with the sagital alignment of the lombo-pelivien complex (post-infarctus care, cardiac insufficiency)

Exclusion Criteria:

- The patient is participating in another study

- The patient is in an exclusion period determined by a previous study

- The patient is under judicial protection, under tutorship or curatorship

- The patient refuses to sign the consent

- It is impossible to correctly inform the patient

- The subject has had more than two x-rays, or similar ray exposure during the previous year

- The subject has a professional activity or hobby that exposes him/her to radiation

- The subject has a lombo-pelivien malformation

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
Sagital xrays
5 xrays will be taken: (1) Upright standing position; (2) Upright, straight chair position; (3) Slouching, straight chair position; (4) Upright, ergonomic chair position; (5) Slouching, ergonomic chair position.

Locations

Country Name City State
France Centre Hospitalier Universitaire de Nîmes Nîmes Cedex 09 Gard

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nimes

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary % variation in the pelvic incidence angle in sitting compared to standing Upon xray; day 1 No
Secondary % variation in the sacral slope angle in sitting compared to standing upon xray; Day 1 No
Secondary % variation in the pelvic tilt angle in sitting compared to standing upon xray; Day 1 No
Secondary % variation in the lumbar lardosis angle in sitting compared to standing upon xray; Day 1 No
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