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Educational Interventions to Reduce Concerns About Falling, Falls and Associated Outcomes Among Older Adults

Effectiveness of Educational Interventions to Reduce Concerns About Falling, Falls and Associated Outcomes Among Older Adults: a Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07515053
Enrollment
102
Registered
2026-04-07
Start date
2026-04-15
Completion date
2027-03-01
Last updated
2026-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Concerns About Falling, Fall Prevention, Falls

Keywords

concerns of falling, falls, older adults, clinical trial, educational intervention, active methods of teaching

Brief summary

The goal of this clinical trial is to learn if an active educational intervention (using interactive and active methods of teaching) works better than the traditional lecture teaching to reduce concerns of falling, falls and other health problems among older adults. The main questions it aims to answer are: Does having more dynamic interactive educational interventions can performed better than using just traditional lectures? Are these interventions able to reduce concerns of falling, fears and other outcomes among older adults? Participants will: Receive one of the interventions (active/interactive or traditional lecture) Answer self-report questionnaires related to concerns of falls and falls Perform some fall-related tests Be followed for 3 and 6 months

Detailed description

Previous studies and meta-analyses have shown that educational strategies for fall prevention are still underexplored and have produced inconsistent results, possibly due to the limited use of appropriate educational methods and approaches that effectively change older adults' perceptions and behaviors related to falls. This study aims to investigate the effects of a six-week educational intervention using active learning methodologies on concern about falling in community-dwelling older adults compared to a control group. Our secondary objectives are to evaluate whether the educational intervention reduces fall events and near-fall events and improves knowledge and awareness related to fall prevention in older adults. This is a randomized, parallel-group trial in which participants will be allocated to either an interactive educational intervention group (active methods of teaching) or a control group receiving the same educational content through printed materials and a lecture on general healthy aging. Follow-up assessments will be conducted immediately after the intervention period (6 weeks), and at 3 months and 6 months after the intervention. Falls and near-falls will be monitored throughout the follow-up period using follow-up contacts.

Interventions

BEHAVIORALInteractive Fall Prevention Education

Arm/Group Experimental: Interactive Fall Prevention Education Arm Description: The intervention will be carried out in groups of 12 to 17 participants. There will be six educational sessions (delivered once a week) focusing on the following fall prevention topics: (1) impact of falls and aging-related changes; (2) identification of fall risk and protective factors; (3) home safety and environmental modifications; (4) fall prevention strategies; (5) concern about falling and what to do after a fall; and (6) adoption of safe behaviors and fall prevention strategies. At each session, participants will receive printed educational materials summarizing the main topics discussed (these materials are the same offered to the control group). The intervention will use interactive and active teaching methods, including group discussions, games, simulated scenarios, problem-solving activities, and practical examples. The educational content will be based on fall prevention guidelines from the Cent

The control group will receive a lecture on general healthy aging (not related to falls) and printed educational leaflets covering the same six fall prevention topics addressed in the interactive educational intervention, including fall risk factors, home safety, prevention strategies, and what to do after a fall. The educational content will be delivered only through printed materials and not through interactive sessions.

Sponsors

Federal University of Juiz de Fora
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Intervention model description

This is a randomized, parallel-group trial in which participants will be allocated to either an interactive educational intervention group (active methods of teaching) or a control group receiving the same educational content through printed materials and a lecture on general healthy aging. Outcomes will be assessed at baseline and follow-up timepoints.

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participants with 60 years old or older * At least one fall in the previous 12 months. * A minimum score for the Mini-Mental State Examination (MMSE) according to educational level: Illiterate: 13, 1 to 7 years of schooling: 18, More than 7 years of schooling: 26

Exclusion criteria

* MMSE score below the minimum cutoff for educational level. * Current participation in regular physical therapy treatment. * Presence of severe neurological, motor, and/or visual impairments that may interfere with participation in the study. * Refusal or inability to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Concern about FallingBaseline, 6 weeks, 3 months, and 6 monthsConcern about falling will be measured using the Falls Efficacy Scale International (FES-I). Scores range from 16 to 64, with higher scores indicating greater concern about falling

Secondary

MeasureTime frameDescription
Proportion of participants with at least one fallBaseline, 6 weeks, 3 months, and 6 monthsThe proportion of participants who experience at least one fall during the follow-up period will be recorded using follow-up contacts
Number of FallsBaseline, 6 weeks, 3 months, and 6 monthsThe total number of falls will be recorded during the follow-up period using follow-up contacts.
Knowledge about fall preventionBaseline, 6 weeks, 3 months, and 6 monthsChange in knowledge about fall prevention will be assessed using the Falls Risk Awareness Questionnaire (FRAQ-Brazil), which evaluates knowledge about fall risk factors, prevention strategies, and situations associated with fall risk. Higher scores indicate greater knowledge related to fall prevention.
Fall risk awarenessBaseline, 6 weeks, 3 months, and 6 monthsChange in fall risk awareness will be assessed using the Falls Risk Awareness Questionnaire (FRAQ-Brazil), which evaluates participants' awareness and perception of fall risk factors and situations associated with falls
Number of near-fallsBaseline, 6 weeks, 3 months, and 6 monthsThe total number of near-falls during follow-up will be recorded using follow-up contacts. A near-fall will be defined as an event in which the participant slips, trips, or loses balance but is able to prevent coming to rest on the ground, floor, or lower level.
Proportion of participants with at least one near-fallBaseline, 6 weeks, 3 months, and 6 monthsThe proportion of participants who experience at least one near-fall during follow-up will be recorded using follow-up contacts. A near-fall will be defined as an event in which the participant slips, trips, or loses balance but is able to prevent coming to rest on the ground, floor, or lower level.

Countries

Brazil

Contacts

CONTACTJordania L Almas, PT, MSc
jordaniaalmas@yahoo.com.br+55 32 98875-0633
CONTACTAlessandra LG Lucchetti, MD, PhD
alessandra.lucchetti@ufjf.br

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 10, 2026