ITMO public health
Last update : 07/06/2015 | Version : 1 | ID : 9162
| General | |
| Identification | |
| Detailed name | Case-Control Study on Osteoporosis Prevention By Vibration Therapy |
| Sign or acronym | vibrOs |
| CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation | CNIL (declaration of conformity to MR001): 1167710; CPP notification date: 07/01/2009; 07/01/2009; AFFSAPS approval date: 05/02/2010 |
| General Aspects | |
| Medical area |
Disability/handicap Geriatrics Physical medicine and rehabilitation Radiology and medical imaging Rheumatology |
| Keywords | vibration, vibrating "power plate" platform, bone mass, incidence |
| Scientific investigator(s) (Contact) | |
| Name of the director | Vico-Pouget |
| Surname | Laurence |
| Address | 15 rue Ambroise Pare 42023 ST ETIENNE CEDEX 2 |
| Phone | +33 (0)4 77 42 18 57 |
| vico@univ-st-etienne.fr | |
| Unit | U1059 Biologie intégrative du tissu osseuxÉquipe/activité :Contraintes mécaniques et tissu osseux- Métabolisme énergétique et os |
| Organization | Inserm ; CHU de Saint-Etienne ; Université Jean |
| Collaborations | |
| Funding | |
| Funding status |
Public |
| Details | - IFRESIS - Federal Scientific Research and Health Engineering Institute (Institut fédératif de recherche en sciences et ingénierie de la santé) - French National Institute of Health and Medical Research. |
| Governance of the database | |
| Sponsor(s) or organisation(s) responsible | Institut national de la santé et de la recherche médicale - Inserm |
| Organisation status |
Public |
| Sponsor(s) or organisation(s) responsible | CHU de Saint-Etienne |
| Organisation status |
Public |
| Sponsor(s) or organisation(s) responsible | Université Jean Monnet |
| Organisation status |
Public |
| Sponsor(s) or organisation(s) responsible | Institut fédératif de recherche en sciences et ingénierie de la santé - Ifresis |
| Organisation status |
Public |
| Additional contact | |
| Main features | |
| Type of database | |
| Type of database |
Study databases |
| Study databases (details) |
Case control study |
| Database recruitment is carried out by an intermediary |
A selection of health institutions and services |
| Database recruitment is carried out as part of an interventional study |
No |
| Additional information regarding sample selection. | Recruitment takes place about every 4 months; female volunteers are identified following a selection visit. |
| Database objective | |
| Main objective | To highlight the positive impact of professional vibrating platforms on bone fragility. |
| Inclusion criteria |
- Female;
- Aged between 55 and 75 years old; - Sedentary (less than 2 hours physical activity per week); - Bone fragility not treated with medication. |
| Population type | |
| Age |
Adulthood (45 to 64 years) Elderly (65 to 79 years) |
| Population covered |
General population |
| Gender |
Woman |
| Geography area |
National |
| Detail of the geography area | France |
| Data collection | |
| Dates | |
| Date of first collection (YYYY or MM/YYYY) | 05/2010 |
| Size of the database | |
| Size of the database (number of individuals) |
< 500 individuals |
| Details of the number of individuals | 240 - 120 cases - 120 controls. |
| Data | |
| Database activity |
Current data collection |
| Type of data collected |
Clinical data Paraclinical data Biological data |
| Clinical data (detail) |
Direct physical measures |
| Paraclinical data (detail) | Bone function test, high-resolution ankle and wrist scan, calculation of muscular and postural strength, as well as control and balance. |
| Biological data (detail) | Blood sample with bone markers. |
| Presence of a biobank |
Yes |
| Contents of biobank |
Whole blood |
| Details of biobank content | Bone markers. |
| Health parameters studied |
Health event/morbidity |
| Procedures | |
| Data collection method | The "case" group consists of three 15-minute sessions per week on the Power Plate platform, supervised by a coach, at a rate of 130 sessions over 12 months. All sports activity shall be stopped for the following six months to see if the benefits remain. The control group does not participate in any session. |
| Participant monitoring |
Yes |
| Details on monitoring of participants | Follow-up for 18 months with medical checkpoints every 6 months. |
| Links to administrative sources |
No |
| Promotion and access | |
| Promotion | |
| Link to the document | http://www.ncbi.nlm.nih.gov/pubmed/1627903 |
| Access | |
| Terms of data access (charter for data provision, format of data, availability delay) | Contact the scientist in charge. |
| Access to aggregated data |
Access on specific project only |
| Access to individual data |
Access on specific project only |
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