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Accidental FallsCPNCT00512655

Trial to Reduce Falls Incidence Rate in Frail Elderly

A study testing Fall prevention course in people with Accidental Falls, run by Radboud University Medical Center at 3 sites in Netherlands.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

Background: Approximately 750,000 elderly Dutch people fall at least once a year, which often results in physical injuries and a fear of falling, with high costs and far-reaching consequences on functionality, physical activity, quality of life and mental well-being. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Accidental Falls
What is being tested?
Fall prevention course
Could I receive a placebo?
No, everyone receives an active treatment
How many people
320 participants
Where
3 sitesNetherlands
Study dates
Jan 2008to Mar 2010
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • At least one fall in the last 6 months
  • Living in their own home or in a home for the aged
  • Availability of a primary caregiver caring for the patient at least once a week
  • Ability to walk 15 meters independently (use of a walking aid is permitted)
  • Life expectancy of more than 6 months, as judged by their geriatrician

Who cannot join

  • Dyads of patients and caregivers in whom outcome assessment is highly unlikely to succeed, for example because they proved not to be able to register falls in the three months before randomization, will be excluded
  • MMSE score of less than 15
  • On the waiting list for a nursing home

Trial locations and contacts

3 sites in 1 country.

Netherlands3 sites
  • Rijnstate Ziekenhuis

    Arnhem

  • Radboud University Nijmegen Medical Centre

    Nijmegen, Gelderland, 6500 HB

  • CWZ

    Nijmegen

Other trials in Netherlands

About this study

Official title: Randomized Controlled Trial to Reduce Falls Incidence Rate in Frail Elderly

Background: Approximately 750,000 elderly Dutch people fall at least once a year, which often results in physical injuries and a fear of falling, with high costs and far-reaching consequences on functionality, physical activity, quality of life and mental well-being. Falling is not only a burden for patients, it is also a burden for their caregivers. Recurrent falling is a complex problem. However, the pathophysiological background of falls, gait problems and dementia is largely unknown. The general pathophysiological hallmark of aging is a liability in homeostatic mechanisms of organs. This liability results in an impaired ability to adapt to stress and in increased biological variation in outcome measures within individuals. In this study the investigators aim at developing an intervention to reduce recurrent falling in frail elderly fallers.

Hypotheses: The investigators hypothesize that the intervention program will decrease the number of falls and fear of falling and increase mental well-being, physical activity and functional performance in frail elderly people with a history of recurrent falling. In addition, the burden on the caregivers will be reduced due to the intervention and will be cost-effective. Furthermore, the investigators hypothesize that patients with a high short-term intra-individual biological variability in gait and cognition variables have a higher risk of falling, worse gait performance and cognitive decline after long term follow-up.

Read more

Study Design: Randomized, controlled, single-blind trial.

Study Population: 160 patients referred to a geriatric outpatient clinic, who fell at least once in the last 6 months and their primary caregivers (N=160).

Intervention: A multifaceted fall prevention program for frail elders to reduce falls incidence rate, consisting of physical and cognitive components. Moreover, it includes a training program for caregivers in which they learn to support and give advice to the patients, aiming to decrease the burden on the caregivers.

Primary Outcome Measures: The fall incidence rate is the primary outcome measure. Total observation time of falls will be 6 months after the start of the intervention.

Secondary Outcome Measures: In the patients, the secondary outcome measures are fear of falling (FES), quality of life (MOS-20), depression and general anxiety, functional performance in activities of daily living, physical activity, mobility, gait parameters, body sway and biomarkers of endothelial function and frailty. For the caregiver, the secondary outcome measures are caregiver's burden, mood and quality of life. In addition, intraindividual variability of cognition, balance and gait in both patients and caregivers, will be assessed and cost-effectiveness of the intervention will also be determined.

Read the detailed description

Nature and Extent of the Burden and Risks Associated with Participation, Benefit and Group Relatedness: The outcome of this study may have important reflections on protocols to prevent falling among elders and on health care decision makers to stimulate starting new fall clinics and implement these protocols. Through this study, the well-being and functionality of frail elders and their caregivers could be improved. As falling has an enormous economic burden, a new effective fall prevention intervention could reduce health care costs substantially. The tests consisting of questionnaires and gait and balance measurement are non-invasive and safe. Taking blood samples is an invasive procedure, although no serious adverse effects are expected. There are no foreseeable risks associated with participation in this study. However, a burden will be placed on participating individuals because the training sessions and measurements are time-consuming.

Being tested
Fall prevention course
Keywords
Fear of falling, Intraindividual variability, Cognition, Fall prevention, Fear, Frail elderly, Intervention

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Fall prevention courseBehavioural

    Duration: 5 weeks, 2 sessions of 2 hours per week: 10 sessions in total.

Study groups in NCT00512655
Study groupRoleWhat they receive
1ExperimentalIntervention: 5 week training program, 2 sessions per week (total of 10 sessions). Training includes both the patient and the caregiver. The training consists of two components: a cognitive and a physical component.
Receives: Behavioral: Fall prevention course
2No interventionUsual care.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Falls incidence rate

    Measured: 6 months

Secondary outcomes (12)
  1. Burden for the caregiver

    Measured: 4 measurements within 6 months

  2. Quality of life (MOS-20)

    Measured: 4 measurements within 6 months

  3. Balance confidence

    Measured: 4 measurements within 6 months

  4. Depression and general anxiety

    Measured: 4 measurements within 6 months

  5. Functional performance and activities of daily living

    Measured: 4 measurements within 6 months

  6. Mood

    Measured: 4 measurements within 6 months

  7. Physical activity

    Measured: 4 measurements within 6 months

  8. Mobility

    Measured: 4 measurements within 6 months

  9. Balance

    Measured: 4 measurements within 6 months

  10. Cognition

    Measured: 4 measurements within 6 months

  11. Fear of falling (FES)

    Measured: 4 measurements within 6 months

  12. Mental well being

    Measured: 4 measurements within 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Aug 2007 (estimated)
  2. Study startJan 2008
  3. Primary completionMar 2010
  4. Study completionMar 2010

Why it stopped: Extremely difficult recruitment. Preliminary analysis showed no effect of the intervention.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
320 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00512655
Sponsor's protocol ID
CP MM 19-08-12-05-30-08
Other IDs
SNO-T-0601-60, ZonMw 920-03-457
Acronym
CP
Status last verified
Jun 2010
First submitted
7 Aug 2007
Last updated
7 Jul 2010
Results posted
No
Data monitoring committee
No

Publications

  • Faes MC, Reelick MF, Melis RJ, Borm GF, Esselink RA, Rikkert MG. Multifactorial fall prevention for pairs of frail community-dwelling older fallers and their informal caregivers: a dead end for complex interventions in the frailest fallers. J Am Med Dir Assoc. 2011 Jul;12(6):451-8. doi: 10.1016/j.jamda.2010.11.006. Epub 2010 Dec 24.

    PubMed 21450224

Questions about this trial

What is this clinical trial studying?

A study testing Fall prevention course in people with Accidental Falls, run by Radboud University Medical Center at 3 sites in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 7 Jul 2010. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Extremely difficult recruitment. Preliminary analysis showed no effect of the intervention.). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Falls incidence rate (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00512655, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Jul 2010.

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