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Recruiting Not applicable

Comparison of Focus of Attention in Virtual Reality-Based Exercise Training in Older Adults With Low Back Pain

NCT07414017 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-02-23
Last updated
2026-02-27

Condition(s) studied

Focus of Attention

Investigational drug(s) / intervention(s)

Traditional treatment programExternal Focus of Attention Virtual Reality ExerciseInternal Focus of Attention Virtual Reality Exercise

Traditional treatment program: The study will be conducted over a total of 6 weeks, with sessions held 3 days per week. Each session will last approximately 45-60 minutes. All participants will undergo a virtual reality-assisted core stabilization exercise program under the supervision of a physical therapist in a safe environment. The following basic core stabilization exercises will be performed in both groups: * Diaphragmatic breathing and abdominal bracing * Pelvic tilt (posterior/anterior) * Bridge exercise * Opposite arm-leg lift in quadrupedal position * Seated and standing trunk stabilization exercises * Dynamic balance and weight transfer exercises

External Focus of Attention Virtual Reality Exercise: Participants in this group will receive a structured virtual reality-based core stabilization exercise program accompanied by verbal and visual instructions designed to direct attention toward the effects of movement on the environment, task outcomes, and externally defined targets within the virtual environment.

Internal Focus of Attention Virtual Reality Exercise: Participants in this group will receive the same structured virtual reality-based core stabilization exercise program, accompanied by verbal and visual instructions aimed at directing attention toward body segment positioning, trunk control, muscle activation, and internal components of movement.

Study summary

Chronic low back pain is highly prevalent among older adults and is associated with impaired balance, increased fall risk, frailty, depressive symptoms, and reduced functional capacity. Exercise-based rehabilitation is a cornerstone of management in this population, and emerging evidence suggests that attentional focus strategies may influence motor learning and functional outcomes. Virtual reality-based exercise interventions provide an interactive and engaging environment that may further enhance rehabilitation outcomes in older individuals.

The purpose of this randomized controlled trial is to compare the effects of external and internal focus of attention strategies applied during a virtual reality-based core stabilization exercise program on frailty, balance, fall risk, lower extremity functional strength, sarcopenia risk, and depression in older adults with chronic low back pain.

Participants will be randomly allocated to either an external focus or internal focus group. Both groups will receive the same virtual reality-based core stabilization exercise program, administered three times per week for six weeks under physiotherapist supervision in a safe clinical setting. The exercise content, session duration, exercise volume, and progression will be identical between groups; the only difference will be the verbal and visual instructions provided to direct participants' attentional focus.

Outcomes will be assessed at baseline and after the intervention period. Frailty will be evaluated using the Frailty Assessment Scale (FAS-TR), sarcopenia risk using the SARC-T questionnaire, balance and fall risk using the Biodex Balance System, functional lower extremity strength using the Five Times Sit-to-Stand Test, and depressive symptoms using the Beck Depression Inventory. This study aims to determine whether attentional focus strategies differentially influence clinical and functional outcomes in older adults with chronic low back pain undergoing virtual reality-based exercise training.

Eligibility

Sex
ALL
Min age
65 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Aged 65 years and older * Diagnosis of non-specific chronic low back pain lasting at least 3 months * Ability to stand and walk independently (use of assistive devices such as a cane or walker is permitted) * Ability to perform most activities of daily living independently * No severe visual, auditory, or vestibular impairments that would prevent participation in a virtual reality-based exercise program * Adequate cognitive function to understand and follow instructions (Mini-Mental -State Examination score ≥ 24 or clinical judgment) * Willingness to participate in the study and provision of written informed consent Exclusion Criteria: * Presence of specific causes of low back pain (e.g., vertebral fracture, tumor, infection, inflammatory rheumatic diseases, advanced spinal stenosis, spondylolisthesis) * History of lumbar spine or lower extremity surgery within the past 6 months * Presence of severe neurological disorders (e.g., stroke, Parkinson's disease, multiple sclerosis) or severe peripheral neuropathy * Uncontrolled cardiovascular, respiratory, or metabolic diseases that may pose a risk during exercise participation * Any acute medical condition or musculoskeletal disorder that contraindicates participation in exercise training

Primary outcome measure(s)

  • Frailty Level — 6 week
    Frailty will be assessed using the Frailty Assessment Screening Tool (FAST-TR). FAST-TR is a validated and reliable screening instrument designed to identify frailty risk in older adults and includes physical, functional, and psychosocial components. Higher scores indicate greater frailty risk.
  • Balance Performance — 6 week
    Static and dynamic balance performance will be objectively assessed using the Biodex Balance System. The Biodex Balance System is a valid and reliable device widely used to evaluate postural control in older adults. Static balance will be assessed using the Postural Stability Test, which measures overall, anterior-posterior, and medial-lateral stability indices. Dynamic balance will be evaluated using the Limits of Stability (LOS) test, which assesses the participant's ability to voluntarily control their center of gravity within their base of support..
  • Fall risk — 6 week
    Fall risk will be evaluated using the Fall Risk Test protocol of the Biodex Balance System. This test objectively quantifies the individual's risk of falling by measuring balance performance on an unstable platform under standardized conditions. The Biodex Fall Risk Index provides an overall score, with higher scores indicating greater fall risk.

Trial sites (1)

FacilityCityRegionStatus
Kirşehir Ahi Evran Univercity Center Kirşehi̇r Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07414017 on ClinicalTrials.gov ↗ ← All trials in Turkey