NCT07522827

Brief Summary

This study will be conducted to evaluate whether the foot and ankle proprioceptive exercise program contributes to foot posture, physical performance and fall incidence in geriatric individuals. Through this research, as a result of physiological changes that occur as age increases, foot posture and physical performance in geriatric individuals are negatively affected, and the incidence of falls increases, causing injuries. It is expected to achieve changes in foot posture, physical performance and fall incidence with the foot and ankle proprioceptive exercise program in geriatric individuals.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2023

Geographic Reach
1 country

1 active site

Status
completed

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

January 24, 2023

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 10, 2024

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2024

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

July 17, 2025

Completed
9 months until next milestone

First Posted

Study publicly available on registry

April 13, 2026

Completed
Last Updated

April 13, 2026

Status Verified

March 1, 2026

Enrollment Period

1.4 years

First QC Date

July 17, 2025

Last Update Submit

April 4, 2026

Conditions

Keywords

geriatricfootexercise

Outcome Measures

Primary Outcomes (1)

  • Physical Performance

    Short Physical Performance Battery (SPPB)

    Baseline, 8 weeks (Post-intervention), and 3 months (Follow-up).

Study Arms (2)

Intervention group

EXPERIMENTAL

Due to the high risk of mortality and morbidity associated with the elderly population, it is planned that the study will be conducted with 20 participants in the intervention group and 20 participants in the control group. For group randomization, stratification will be based on age and gender, as these factors are considered potential influencers of fall risk among geriatric individuals included in the sample. Participants in each study group will be stratified according to these two criteria. In addition, each participant will be assigned a unique identification number for tracking and confidentiality purposes.

Other: Foot and ankle proprioceptive exercise

control grup

EXPERIMENTAL

The control group will only receive the home program.

Other: home exercise

Interventions

group receives a home program.

control grup

Foot and ankle proprioceptive exercises will be performed only while seated. This is because, in geriatric individuals at risk of falling, the aim is to reduce the risk of falls by conducting exercises in a safe environment.

Intervention group

Eligibility Criteria

Age65 Years - 100 Years
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

  • Individuals aged 65 years and older
  • A score of 24 or higher on the Standardized Mini-Mental State Examination (MMSE)
  • Ability to read and write in Turkish
  • Voluntary participation in the study with signed informed consent
  • Ability to stand independently and take at least two steps without assistance
  • Ability to walk independently in the community without the use of lower extremity orthoses or

You may not qualify if:

  • Uncorrected visual impairments that cannot be resolved with glasses
  • Uncorrected hearing loss despite the use of hearing aids
  • A score of 23 or below on the Mini-Mental State Examination
  • Any surgical procedure affecting balance within the last 6 months
  • Presence of deformities in the lumbar spine, hip, or knee joints
  • Lower extremity amputation
  • Malignancy involving the lower extremities
  • Diagnosis of moderate to severe congenital heart disease, coronary artery disease, or cerebrovascular disease
  • Any medical contraindications to exercise
  • Inability to establish cooperation with the participant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara University, Haymana Vocational School

Ankara, Haymana, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • bahar anaforoğlu, prof

    bidb@aybu.edu.tr

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
SEQUENTIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PHYSİCAL THERAPİST

Study Record Dates

First Submitted

July 17, 2025

First Posted

April 13, 2026

Study Start

January 24, 2023

Primary Completion

June 10, 2024

Study Completion

June 15, 2024

Last Updated

April 13, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations