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RecruitingNCT07622095MOB-SCOREUpdated Sep 3, 2026

Validation of the French Version of the New Mobility Score (NMS)

An observational study in Hip Fractures, Mobility Limitation and Independence, sponsored by Hospices Civils de Lyon. Recruiting at 1 site in France. Open to participants aged 75 Years and older. Per ClinicalTrials.gov, last updated 2026-09-03.

Sponsored by Hospices Civils de Lyon · Observational

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
75 Years and older
Sex
All
01

Study summary

The incidence of hip fractures in France is 50,000 cases per year among women and 16,000 among men, with a 1-year mortality rate of 20-24%. After a fracture, 10-30% of patients become functionally dependent. The increasing aging of the population and the rise in dependency are likely to worsen the situation of older patients in hospital settings.

Several tools are available to assess functional independence, including the New Mobility Score (NMS), which evaluates mobility through three domains: mobility indoors, mobility outdoors, and shopping activities. The NMS has shown good performance in predicting patient mortality and functional recovery, and its use is recommended in clinical practice. However, the French version of the NMS has not yet been validated.

The French validation of the NMS is important to facilitate its implementation in clinical practice and research, particularly because of its simplicity and the need for rapid assessment tools for healthcare professionals. A French version of the NMS has been translated, and the MOB-SCORE study aims to assess its reliability and validity among healthcare professionals caring for patients with hip fractures.

02

Conditions studied

  • Hip Fractures
  • Mobility Limitation
  • Independence
  • Autonomy

Keywords

  • New Mobility Score
  • Validation
  • Inter-rater reliability
03

In context

Hip Fractures

842 studies on the registry are indexed under Hip Fractures; 165 are open to participants now.

This study's planned enrollment of 100 is below the median of 149 across 280 observational studies indexed under Hip Fractures.

Browse Hip Fractures studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,866 studies on the registry; 448 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
75 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Subjects admitted to a hospital ward following a hip fracture

Eligibility criteria

Inclusion Criteria:

  • Patients aged 75 years and older admitted to a hospital department following a hip fracture and treated surgically (osteosynthesis or arthroplasty).
  • Type of fracture: pertrochanteric fracture or femoral neck fracture.
  • Sufficient proficiency in French to complete the questionnaires.
  • Patients affiliated with a health insurance scheme.
  • No objection to participate from the patient or the caregiver in case of cognitive impairment.

Exclusion Criteria: no exclusion criteria

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • Subjects aged 75 years and over admitted to a hospital ward following a hip fracture

    Subjects aged 75 years and over, admitted to a hospital service following a hip fracture (per trochanteric or femoral neck) and having received surgical treatment (osteosynthesis or arthroplasty).

    Other: Questionnaires

Interventions

  • OtherQuestionnaires

    New Mobility Score (NMS), Measure of Functional Independence (MIF), Cumulated Ambulation Score (CAS), Mini-Mental State Examination (MMSE).

06

What researchers measure

Primary outcomes

  1. Inter-rater reliability of the New Mobility Score (NMS)

    The New Mobility Score (NMS) assesses mobility in three domains (indoors, outdoors, and while shopping). For each domain, a score ranging from 0 (unable to perform the task) to 3 (able to perform the task independently) is assigned, with a total score ranging from 0 to 9. A score of ≤6 indicates functional impairment, whereas a score of \>6 indicates a high pre-fracture level of mobility in patients with hip fracture. The NMS will be rated by a physiotherapist and an adapted physical activity (APA) instructor.

    Time frame: Within 7 days following the fracture surgery

Secondary outcomes

  1. Internal consistency of the New Mobility Score (NMS)

    Internal consistency of the New Mobility Score (NMS) items.

    Time frame: Within 7 days following the fracture surgery

  2. Convergent validity of the New Mobility Score (NMS) with other functional independence scales, cognitive status and age.

    Correlation between the New Mobility Score (NMS) and: * Measure of Functional Independence (MIF): 18 items assessing 6 functional domains. Each item is scored from 1 (total assistance) to 7 (complete independence). The total score ranges from 18 to 126. * Cumulated Ambulation Score (CAS): independence in 3 activities (getting in and out of bed, sitting down and rising from a chair, walking ability). Each activity is scored on a scale from 0 (unable despite human assistance) to 2 (able without human assistance), with a total score ranging from 0 to 6 (6 indicating independent ambulation). * Mini-Mental State Examination (MMSE): 30 questions divided into 6 categories. For each question, a correct answer scores 1 point (0 otherwise), with a total score ranging from 0 to 30. * Age

    Time frame: Within 7 days following the fracture surgery

  3. Predictive validity of mortality at postoperative day 30.

    Correlation between the New Mobility Score (NMS) and vital status at postoperative day 30.

    Time frame: Within 30 days following the fracture surgery

  4. Discriminatory validity based on place of residence.

    Comparison of the New Mobility Score (NMS) according to pre-fracture living arrangements: living alone versus living in a nursing home/with family.

    Time frame: Within 7 days following the fracture surgery

07

Study locations

1 of 1 sites recruiting
  • Service I3 de court séjour gériatrique, Hôpital de la Croix-Rousse, Hospices Civils de Lyon
    Lyon, 69004, France
    Recruiting
    • Iago HUGHES SANMARTIN, Physiotherapist · ContactIago.hughes-sanmartin@chu-lyon.fr · (0)4 26 10 94 75
    • Iago HUGHES SANMARTIN, Physiotherapist · Principal investigator
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07622095
Responsible party
Sponsor
First posted
Jun 2, 2026
Start date
Aug 27, 2026
Primary completion
Feb 2028 (estimated)
Completion
Mar 2028 (estimated)
Last update
Sep 3, 2026

Study contacts

Olivia FEBVEY-COMBES, MD
Contact
olivia.febvey-combes@chu-lyon.fr
(0)4 72 11 51 62 ext. +33

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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