Effectiveness of Three Interventions to Reduce Fear of Falling and Improve Functionality in the Elderly

July 5, 2017 updated by: Universidad de Caldas

Randomized Clinical Trial Evaluating the Effectiveness of Three Interventions Programs to Improve Functionality and Decrease Fear of Falling in the Elderly

Fear of falling is a major health problem among community-dwelling older adults that may contribute to avoidance of activities that they are capable of performing. Studies show that the fear of falling may lead to a continual, complex decline in older adults that includes a loss of auto efficacy, restriction of physical activities and social participation, physical frailty, falls and disability. Apart from these effects, the fear of falling may also have financial implications for health care systems and the general public. Several interventions have been shown to reduce fear of falling with multifactorial interventions, including physical and behavioral components, being most successful. Behavioral components usually comprise strategies to reduce catastrophic thinking and fear-related avoidance behaviors while physical components usually comprise falls prevention exercise programs. However, multifactorial programs are not always feasible or preferred by older people. In this framework, the objective of this works is to assess the effects (benefits and effectiveness) of three interventions programs (Tai Chi, postural control exercises and behavioral therapy intervention) to improve functionality and decrease fear of falling in older people living in the community.

Study Overview

Detailed Description

Fear of falling is common among elderly people. Fear of falling can be associated with reductions in physical and social activities and negative impacts on quality of life. Several interventions have been shown to reduce the fear of falling, but their effectiveness has not been compared. The objective of this study is to evaluate the effectiveness of three interventions programs to improve functionality and decrease fear of falling in the Elderly. Effective interventions to lessen fear of falling could therefore have significant consequences for individuals, their families and healthcare delivery systems.

Methods/Design: This is a controlled, randomized clinical trial of individual assignment, carried out on community living elderly, from Manizales (Colombia) who reporting fear of falling with restriction of activities of daily living.

Study Type

Interventional

Enrollment (Anticipated)

110

Phase

  • Not Applicable

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

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

56 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Community-dwelling older people
  • People who reported fear of falling
  • "Leganés Cognitive Test" ≥23
  • SPPB ≤ 9

Exclusion Criteria:

  • Some cognitive affection and/or medical condition that may affect the intervention
  • Permanent use of wheelchair
  • People who have received prior protocolized management for fear of falling

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

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Cognitive behavioural therapy
The program aims to teach participants how to deal with their concerns about falls and related avoidance of activity, in order to increase their physical, social and functional activities. The cognitive behavioural intervention program, provides by psychologists, consists of eight group sessions, 60 minutes each. During each session a main theme is addressed. The themes of the program are: concerns about falls; thoughts about falling; physical exercise; asserting oneself; overcoming personal barriers; safe behaviour; and managing concerns about falls.
The program aims to teach participants how to deal with their concerns about falls and related avoidance of activity
Active Comparator: Tai chi
Subjects in the Tai Chi group undertook supervised Tai Chi training in the Yang style of 24 movements, for one hour, once a week for 8 weeks. The first 5 min was allocated for warm-up, with the rest of the time for Tai Chi practice.
Tai Chi training in the Yang style of 24 movement
Active Comparator: Postural control exercise
Individually adjusted progressive and specific postural control training, provided by physiotherapists for one hour, one time per week for 8 weeks. The exercise is progressive and specific to functional postural control tasks. It comprises elements that represent activities included in, and required for, independent daily living, such as maintaining balance when sitting, standing and walking; and also reacting to loss of balance.
Individually adjusted progressive and specific postural control training,

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fear of falling
Time Frame: Prospective change from baseline to end of intervention (8 weeks)
Fear of falling is evaluated using Falls Efficacy Scale International questionnaire
Prospective change from baseline to end of intervention (8 weeks)
Functional mobility
Time Frame: Prospective change from baseline to end of intervention (8 weeks)
Functional mobility is evaluated using gait speed and Short Physical performance Battery (SPPB).
Prospective change from baseline to end of intervention (8 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Falls
Time Frame: Prospective change from baseline to end of intervention (8 weeks)
Number of falls in the last year evaluated by open question to the participant
Prospective change from baseline to end of intervention (8 weeks)
Depression
Time Frame: Prospective change from baseline to end of intervention (8 weeks)
Prospective change from baseline to end of intervention (8 weeks) as measured by the scale of Yesavage
Prospective change from baseline to end of intervention (8 weeks)
Handgrip
Time Frame: Prospective change from baseline to end of intervention (8 weeks)
Prospective change from baseline to end of intervention (8 weeks) Measured through the dynamometer
Prospective change from baseline to end of intervention (8 weeks)
Daily life activities
Time Frame: Prospective change from baseline to end of intervention (8 weeks)
Daily life activities at the instrumental level measured through the Lawton and Brody scale
Prospective change from baseline to end of intervention (8 weeks)
Self-Rated Health
Time Frame: Prospective change from baseline to end of intervention (8 weeks)
Subjective assessment of health status by simple dichotomous scale and ordinal scale (Likert scale) with 5 options
Prospective change from baseline to end of intervention (8 weeks)
Postural control
Time Frame: Prospective change from baseline to end of intervention (8 weeks)
under reduced or conflicting sensory conditions and fall risk were investigated, using the Biodex Balance System
Prospective change from baseline to end of intervention (8 weeks)

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Carmen L Curcio, Universidad de Caldas

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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

June 1, 2016

Primary Completion (Anticipated)

August 1, 2017

Study Completion (Anticipated)

December 1, 2017

Study Registration Dates

First Submitted

January 16, 2017

First Submitted That Met QC Criteria

July 5, 2017

First Posted (Actual)

July 7, 2017

Study Record Updates

Last Update Posted (Actual)

July 7, 2017

Last Update Submitted That Met QC Criteria

July 5, 2017

Last Verified

July 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 1386316

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

IPD Plan Description

Data will be available after publication of results. Data will be shared to interested researchers who are planning to perform a meta-analysis. They should write an email to the main contact explaining what type of analysis they will perform and what data they require from the study. Only those data that are considered relevant for the analysis will be shared. Researchers who receive the data should be committed to safeguarding them and complying with and protecting copyright

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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