- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03211429
Effectiveness of Three Interventions to Reduce Fear of Falling and Improve Functionality in the Elderly
Randomized Clinical Trial Evaluating the Effectiveness of Three Interventions Programs to Improve Functionality and Decrease Fear of Falling in the Elderly
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Caldas
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Manizales, Caldas, Colombia, 170004
- Recruiting
- Universidad de Caldas
-
Contact:
- CARMEN L CURCIO, PhD
- Phone Number: 573184665019
- Email: carmen.curcio@ucaldas.edu.co
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Contact:
- Elizabeth PONCE, Psychologist
- Phone Number: 573008789553
- Email: ponce@umanizales.edu.co
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Collaborators
Investigators
- Principal Investigator: Carmen L Curcio, Universidad de Caldas
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
IPD Plan Description
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