Determinants of the Fall Risk Profile and Quality of Life of Older Subjects Visting Climatic Health Resorts

March 2, 2020 updated by: University Hospital, Montpellier

Assessment of the Fall Risk Profile and Quality of Life of Subjects Aged 65 or Older Visiting the French Balaruc-les-bains Climatic Health Resort

The main objective of the study conducted in subjects aged 65 or older visiting the French Balaruc-les-bains climatic health resort was to :

  • Determine factors that distinguish fallers from not fallers
  • Determine factors that may predict falls and injurious falls, 3 and 6 months after the stay in the resort
  • Determine the effects of the 3-week stay in the health resort on quality of life, fear of falling, fatigue, and physical activity

Study Overview

Status

Completed

Conditions

Detailed Description

In all subjects aged 65 or older visiting consecutively the resort over a 5-month period, a questionnaire was administered in order to record:

  • The number of falls and injurious falls in the previous 12 months. Injurious falls are falls complicated by serious or moderate injuries. Falls with serious injuries were those that caused fractures, head injuries requiring admission to hospital, joint dislocations, sprains accompanied by reduced physical function, other non-specified serious joint injuries, and lacerations requiring sutures. Falls with moderate injuries were those that resulted in bruising, sprains, cuts, abrasions, or reduction in physical function for at least three days or in medical help
  • Physical activity over the last 7 days, using the International Physical Activity Questionnaires (IPAQ)
  • Fear of falling, using a visual analogue scale (VAS) (0 to 10).
  • The feeling of fatigue over the previous month, using a visual analogue scale (0 to 10) A questionnaire was administered to record quality of life (EQ-5D-3L), at baseline and 7 days after the end of the stay A questionnaire snt by mail was filled in by subjects 3 and 6 months after the stay in the resort in order to record falls and injurious falls, fatigue, fear of falling, and physical activity (using the above questionnaires).

Physical measurements were performed at the entrance of the health resort :

  • Body height and body weight to the nearest 0.5 cm and 0.1 kg to calculate the body mass index (kg.m-2)
  • The Timed Up and Go test and the time to walk 4 meters at usual pace (Lusardi-2017)
  • The 5 repeated chair stand test
  • The maximum grip strength: using a Camry Electronic Hand Dynamometer
  • The one-leg stand test (lowest value on the right and the left leg), and stand tests feet together, in semi-tandem, and tandem position
  • The score of the Short Physical Performance Battery (SPPB) was calculated based on results of the 4-meter gait speed, and the 5-chair stand and balance tests
  • The Fried's frailty phenotype score was calculated, based on - the weight loss in prior year (body weight at baseline ˗ the self-assessed body weight 12 months before inclusion) (1 point if ≥ 10 lbs lost unintentionally); - muscle strength (1 point if the maximum grip strength was low based on the dynamometer manual); - self-reported fatigue (1 point if Visual Analog Fatigue Scale ≥ 5 in men and ≥ 4 in women), - walking speed (1 point if 4-m walking speed at comfortable pace was in the lowest quintile of values of subjects with the same gender) (≤ 0.71 m.s-1 in women and ≤ 0.76 m.s-1 in men), - physical activities in the previous week (1 point if in the lowest quintile of values of IPAQ of subjects with the same gender) (≤ 2076 MET (Metabolic Equivalent Task) in women and ≤ 2320 MET in men). A total score of ≥ 3 points was indicative of frailty, 1 or 2 points of prefrail phenotype and a score of 0 is indicative of robustness

Study Type

Observational

Enrollment (Actual)

1471

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Montpellier, France, 34295
        • UHMontpellier

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 65 years (ADULT, OLDER_ADULT, CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Subjects (women or men) aged 65 or older who consecutively visited the Balaruc-les-bains health resort for venous or rheumatologic complaints over a 5-month period

Description

Inclusion criteria:

  • Patients aged 65 years or older visiting the Balaruc-les-bains resort for venous or rheumatologic complaints over the 5-month recruitment period
  • Subjects able to comply with all trial procedures
  • Subjects covered by public health insurance
  • Signed informed

Exclusion criteria:

  • Patients with severe physical or neuropsychiatric impairment making impossible the physical measurements at baseline or the reply to the questionnaires at baseline and during the 7 days-, 3 month-, and 6-month follow-up after the stay in the health resort.
  • Subject unable to read or/and write

    • Subject who are in a dependency or employment with the sponsor or the investigator
    • Participation in another clinical trial within the last 4 weeks before the screening date

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of new falls over the folly-up period
Time Frame: 1 year
A fall is defined as an "unexpected event in which the participant comes to rest on the ground, floor, or other lower level" (J Am Geriatr Soc 2011;59:148-57)
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of injurious falls over the folly-up period
Time Frame: at 7 days, 3, and 6 months after the stay in the resort
Number of injurious falls over the folly-up period (El Khoury F, 2015)
at 7 days, 3, and 6 months after the stay in the resort
Fear of falling using a visual analogue scale
Time Frame: at 7 days, 3, and 6 months after the stay in the resort
Fear of falling using a visual analogue scale (VAS) (0 to 10)(Scheffer-2010).
at 7 days, 3, and 6 months after the stay in the resort
Feeling of fatigue using a visual analogue scale
Time Frame: at 7 days, 3, and 6 months after the stay in the resort
the feeling of fatigue using a visual analogue scale (0 to 10)(Wolfe-2004; Hewlett-2011)
at 7 days, 3, and 6 months after the stay in the resort

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

May 1, 2017

Primary Completion (ACTUAL)

May 30, 2017

Study Completion (ACTUAL)

September 30, 2017

Study Registration Dates

First Submitted

February 17, 2020

First Submitted That Met QC Criteria

February 17, 2020

First Posted (ACTUAL)

February 19, 2020

Study Record Updates

Last Update Posted (ACTUAL)

March 5, 2020

Last Update Submitted That Met QC Criteria

March 2, 2020

Last Verified

February 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • RECHMPL16_0129

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

NC

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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