CFC: Falls With Fracture : Role of Cognitive Disorders and Comparison With Bone Fragility

Sponsor
University Hospital, Caen (Other)
Overall Status
Completed
CT.gov ID
NCT02292316
Collaborator
(none)
218
2
2
85.5
109
1.3

Study Details

Study Description

Brief Summary

The purpose of this study is to determine whether cognitive disorders are a risk factor for a fracture after a fall independently of a bone fragility.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: gait and cognitive assessments
  • Biological: blood sample
  • Other: osteodensitometry
N/A

Detailed Description

The fall is a major problem in the elderly. After 65 year old, falls represent 84% of daily living accidents and almost half of the post fall injuries are fractures (Ricard and Thélot, 2007). These falls with fracture lead to a loss of autonomy and a high health cost. Their prevention is a crucial focus of research.

Even if it is obvious that subjects with osteoporosis have a higher risk of fracture than those with a normal bone mineral density, recent studies have shown that most victims of fracture post-fall do not comply with the densitometric definition of osteoporosis.

It is well established that the presence of cognitive disorders, frequent in the elderly, is an important risk factor for falls; It might also be a risk factor for fracture after a fall with an unadapted postural or balance control.

The investigators will test this hypothesis on 150 victims of fracture (upper or lower limb) consecutive to a fall from standing height, recruited in the hospitals of Caen and Rouen (France) in the context of their medical follow-up (with blood and dual energy x-ray absorptiometry [DXA] exams). These patients will be matched to 150 control participants (victims of a fall with no fracture, submitted to the same exams).

All the participants are subjects to an in-depth study of cognitive functions, postural and walking tests and to various scales (daily life activities, depression, ...).

These exams will take half a day, with a two-year follow up (in which the participant will have to note new falls and new medical treatments)

Study Design

Study Type:
Interventional
Actual Enrollment :
218 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Falls With Fracture : Role of Cognitive Disorders and Comparison With Bone Fragility
Actual Study Start Date :
Nov 15, 2011
Actual Primary Completion Date :
Dec 31, 2017
Actual Study Completion Date :
Dec 31, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Fall with fracture

Fall with fracture in the last 6 months; Interventions : behavioral, biological and other; Behavioral intervention includes gait and cognitive assessments Blood sample Osteodensitometry

Behavioral: gait and cognitive assessments
several tests are given in each domain

Biological: blood sample
routine analyses in rheumatology such blood count and 25OH-D

Other: osteodensitometry
Looking for osteoporosis

Sham Comparator: controls

Fall without fracture in the last 12 months; Interventions : behavioral, biological and other; Behavioral intervention includes gait and cognitive assessments Blood sample Osteodensitometry

Behavioral: gait and cognitive assessments
several tests are given in each domain

Biological: blood sample
routine analyses in rheumatology such blood count and 25OH-D

Other: osteodensitometry
Looking for osteoporosis

Outcome Measures

Primary Outcome Measures

  1. Analysis of a global cognitive efficiency score Analysis of bone mineral density [on the inclusion day and two years after]

    MMS, MoCA

Secondary Outcome Measures

  1. Age [on the inclusion day and over two years]

  2. Cognitive scores [on the inclusion day and over two years]

    Mainly tests of memory, attention and executive functions

  3. Fracture features [on the inclusion day and over two years]

    Location and severity

  4. Balance and walking parameters [on the inclusion day and over two years]

    Tinetti scale, TUG and dual-tasks

  5. handgrip force [on the inclusion day and over two years]

    using a dynamometer

  6. Daily life scales scores [on the inclusion day and over two years]

    Mainly IADL

  7. fear of falling [on the inclusion day and over two years]

    ABC-scale

  8. functional restrictions score [on the inclusion day and over two years]

    Lequesne score

  9. Degree of depression [on the inclusion day and over two years]

    MADRS

  10. biological data [on the inclusion day and over two years]

    25OHD

  11. Dual-energy X-ray absorptiometry [on the inclusion day and two years after]

    bone mineral densitometry

Eligibility Criteria

Criteria

Ages Eligible for Study:
55 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Affiliation to the social security system

  • For subjects with fracture : victim of a low-energy fracture of the upper or lower limb that was consecutive to a fall from standing height, and who has accepted to realize a DXA exam in the context of the medical follow-up

  • For control subjects : victim of a fall from standing height, with no fracture, matched in terms of age, sex, socio-cultural level and living space with subjects with fracture.

  • Written informed consent

Exclusion Criteria:
  • Subject who is deprived of liberty, under supervision or legal guardianship

  • Pathology affecting balance (Parkinson's disease, after-effects of stroke, …)

  • Important visual impairment : age-related macular degeneration, …

  • Depressed state

  • Important consumption of alcohol (> 14 drinks per week for women / >21 for men)

  • Subject who is concurrently participating in another clinical study (unless prior notice of the principal investigator)

  • Fall has been caused by a third party (e.g. : pushing), is not from standing height (e.g. : fall from a ladder); fracture is not a low-energy one (e.g. : further a fall during running)

  • For subjects with fracture :

  • The fracture is not consecutive to a fall

  • The fracture is pathological, beyond osteoporosis (e.g. : bone metastases)

  • The last fall responsible for a fracture goes back more than 6 months

  • For control subjects :

o The fall goes back more than 12 months

  • The fall has led to a medical consultation

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Caen France 14000
2 Dr Alain Daragon Rouen France 76000

Sponsors and Collaborators

  • University Hospital, Caen

Investigators

  • Principal Investigator: Christian Marcelli, Professor, CHU of Caen

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Caen
ClinicalTrials.gov Identifier:
NCT02292316
Other Study ID Numbers:
  • RCB 2011A00556-35
First Posted:
Nov 17, 2014
Last Update Posted:
Mar 4, 2020
Last Verified:
Mar 1, 2020
Keywords provided by University Hospital, Caen
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 4, 2020