NCT07775183

Brief Summary

In recent years, exercise programs based on visual stimuli have been reported to improve balance and motor control . However, studies investigating the effects of light-targeted balance training on balance, functional performance, and fear of falling in individuals with a history of falls are limited. The aim of this study is to determine the effects of light-targeted balance training on balance, functional performance, and fear of falling in individuals with a history of falls. In addition, the study aims to investigate whether this training method provides additional benefits compared with traditional balance training. The findings of this study are expected to contribute to the development of rehabilitation programs aimed at preventing falls.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 31, 2026

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

August 15, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 20, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2026

Completed
Last Updated

August 31, 2026

Status Verified

August 1, 2026

Enrollment Period

2 months

First QC Date

August 15, 2026

Last Update Submit

August 27, 2026

Conditions

Keywords

balance trainingrehabilitationfunctional performance

Outcome Measures

Primary Outcomes (1)

  • Change in Balance Performance (Berg Balance Scale)

    Balance performance is assessed using the Berg Balance Scale (BBS). The scale consists of 14 functional tasks scored from 0 to 4. The total score ranges from 0 to 56, where higher scores indicate better balance and lower fall risk.

    Baseline and after 8 weeks of intervention

Secondary Outcomes (6)

  • Change in Functional Mobility (Timed Up and Go Test - TUG)

    Baseline and after 8 weeks of intervention

  • Change in Dynamic Balance (Y-Balance Test)

    Baseline and after 8 weeks of intervention

  • Change in Lower Body Strength (30-Second Chair Stand Test)

    Baseline and after 8 weeks of intervention

  • Change in Gait Speed (10-Meter Walk Test - 10MWT)

    Baseline and after 8 weeks of intervention

  • Change in Fear of Falling (Falls Efficacy Scale-International - FES-I)

    Baseline and after 8 weeks of intervention

  • +1 more secondary outcomes

Study Arms (2)

Experimental Group

EXPERIMENTAL

Participants in this group will receive light-targeted balance training in addition to the standard program.

Behavioral: Light- Targeted Balance Training

Control Group

ACTIVE COMPARATOR

Participants in this group will receive standard balance exercises.

Behavioral: Standard Balance Training

Interventions

Exercises aimed at improving coordination, balance, and functional performance using visual and auditory cues.

Experimental Group

Conventional balance training exercises.

Control Group

Eligibility Criteria

Age18 Years - 95 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • History of at least one fall within the past 12 months
  • Age 18 years or older
  • Ability to walk independently or with an assistive device
  • Ability to understand and follow verbal and visual instructions
  • Voluntary participation in the study and provision of written informed consent by signing the informed consent form

You may not qualify if:

  • Acute orthopedic injury or an active musculoskeletal condition causing pain
  • History of lower extremity surgery within the past 6 months
  • Advanced neurological disorders (e.g., advanced Parkinson's disease, advanced dementia)
  • Severe vestibular dysfunction or significant visual impairment
  • Medical conditions that contraindicate exercise due to severe cardiovascular disease
  • Advanced systemic diseases that severely affect balance

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Uskudar University

Istanbul, Istanbul, 34000, Turkey (Türkiye)

RECRUITING

Central Study Contacts

Shirin Khezritomatari

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 15, 2026

First Posted

August 20, 2026

Study Start

July 31, 2026

Primary Completion

September 30, 2026

Study Completion

September 30, 2026

Last Updated

August 31, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations