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CompletedNCT07841379Updated Oct 13, 2026

Variable vs Fixed Auditory-Cued Stepping Training

An interventional study of Variable-Timing, Variable-Direction Auditory-Cued Stepping Training and Fixed-Timing, Fixed-Direction Auditory-Cued Stepping Training in Sedentary Behavior / Physical Inactivity, Sedentary Healthy Young Individuals and Sedentary Lifestyle, sponsored by Beshoy Maher Rezk Hanna. Completed at 1 site in Egypt. Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by Beshoy Maher Rezk Hanna · Not applicable, Interventional, and Other

Updated Oct 13, 2026Now CompletedFirst site in Egypt+3 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
85
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

This study investigates whether stepping training that uses an unpredictable, variable auditory cue - changing both the timing and the direction of each step - improves dynamic balance and stepping adaptability more than stepping training with a constant, predictable auditory cue. Sedentary young adults will be randomly assigned to one of two 4-week training programs and assessed before and after training.

Read the detailed description

Reduced physical activity is associated with diminished neuromuscular reactivity and postural control. While auditory-cued stepping/gait training has demonstrated benefits for balance and stepping performance in clinical populations (e.g., stroke, Parkinson's disease), evidence in healthy, sedentary young adults remains limited. Motor-learning theory suggests that greater practice variability - in both timing and spatial direction - promotes superior motor adaptation and retention compared with fixed, predictable practice conditions. This randomized controlled trial will compare a combined variable-timing and variable-direction auditory-cued stepping training protocol against a fixed-timing, fixed-direction protocol, in terms of their effects on dynamic balance (Y-Balance Test) and stepping adaptability (Choice Stepping Reaction Time), in sedentary young adults aged 18-35 years, over a 4-week supervised training period.

02

Conditions studied

  • Sedentary Behavior / Physical Inactivity
  • Sedentary Healthy Young Individuals
  • Sedentary Lifestyle

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Keywords

  • auditory cueing
  • stepping training
  • dynamic balance
  • stepping adaptability
  • motor learning
  • contextual interference
  • sedentary young adult
  • rehabilitation
03

In context

Sedentary Behavior

1,273 studies on the registry are indexed under Sedentary Behavior; 300 are open to participants now.

This study's enrollment of 85 is above the median of 60 across 1,076 interventional studies indexed under Sedentary Behavior.

Browse Sedentary Behavior studies →

Lead sponsor

This is the only study on the registry with Beshoy Maher Rezk Hanna as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18-35 years
  • Sedentary lifestyle (International Physical Activity Questionnaire short-form 'inactive/low' category, or \<150 minutes/week of moderate-to-vigorous physical activity)
  • Able to stand and walk independently without an assistive device
  • Normal or corrected-to-normal hearing and vision
  • (BMI) 18.5-29.9 kg/m²
  • Willing and able to provide written and comply with the 4-week training schedule and assessment sessions

Exclusion criteria

Exclusion Criteria:

  • Diagnosed neurological, vestibular, or orthopedic/musculoskeletal condition known to affect balance or gait (e.g., stroke, Parkinson's disease, vestibular disorders, lower-limb fracture/surgery in the past 6 months)
  • History of falls within the past 12 months
  • Hearing impairment or use of a hearing aid/cochlear implant
  • Uncorrected visual impairment
  • Regular participation in structured exercise, sport, or balance/agility training (>150 min/week of moderate-to-vigorous activity)
  • Pregnancy
  • Cardiovascular, respiratory, or other medical to physical exertion/exercise testing
  • Current use of medication known to affect balance, reaction time, or central nervous system function (e.g., sedatives, anti-vertigo medication)
  • Cognitive or communication impairment that would limit the ability to follow auditory-cued instructions
  • Concurrent enrollment in another balance, stepping, or exercise-intervention study
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
85 participants (actual)

Study arms

  • Experimental
    Variable Cueing Group

    Participants will receive auditory-cued stepping training with randomly varying inter-stimulus timing (1.5-3.5 seconds) and randomly varying step direction (anterior, posterior, lateral), 3 sessions/week for 4 weeks.

    Behavioral: Variable-Timing, Variable-Direction Auditory-Cued Stepping Training

  • Active comparator
    Fixed Cueing Group

    Participants will receive auditory-cued stepping training with constant, fixed inter-stimulus timing (every 2.5 seconds) and a single, fixed step direction (forward only), 3 sessions/week for 4 weeks, matched for total training volume with the Variable Cueing Group.

    Behavioral: Fixed-Timing, Fixed-Direction Auditory-Cued Stepping Training

Interventions

  • BehavioralVariable-Timing, Variable-Direction Auditory-Cued Stepping Training

    A supervised stepping-training program delivered 3 sessions/week for 4 weeks (12 sessions total). Each session includes a 5-minute warm-up, 20-25 minutes of auditory-cued stepping training, and a 5-minute cool-down. During the main training phase, participants respond to auditory cues with randomly varying inter-stimulus timing (1.5-3.5 seconds) and randomly varying step direction (anterior, posterior, lateral), stepping onto the cued target as quickly as possible before returning to a central start position.

  • BehavioralFixed-Timing, Fixed-Direction Auditory-Cued Stepping Training

    A supervised stepping-training program delivered 3 sessions/week for 4 weeks (12 sessions total), identical in structure, duration, and total training volume to the Variable Cueing Group. During the main training phase, participants respond to auditory cues delivered at a constant, fixed inter-stimulus interval (every 2.5 seconds) and a single, fixed step direction (forward only), stepping onto the fixed target before returning to a central start position.

06

What researchers measure

Primary outcomes

  1. Change in Y-Balance Test Composite Reach Score

    Dynamic balance assessed using the Y-Balance Test, with composite reach score (anterior, posteromedial, posterolateral directions) normalized to limb length and expressed as a percentage.

    Time frame: Baseline and 4 weeks

  2. Change in Choice Stepping Reaction Time

    Stepping adaptability assessed using Choice Stepping Reaction Time, measured as mean reaction time in milliseconds in response to randomized directional auditory cues.

    Time frame: Baseline and 4 weeks

  3. Change in Choice Stepping Reaction Time

    Stepping adaptability assessed using Choice Stepping Reaction Time, measured as accuracy (percentage of correct responses) in response to randomized directional auditory cues.

    Time frame: Baseline and 4 weeks

Secondary outcomes

  1. Change in Four Square Step Test Time

    Stepping agility and coordination assessed using the Four Square Step Test (FSST), recorded as the time (in seconds) taken to complete a standardized four-directional stepping sequence. Lower scores indicate better performance.

    Time frame: Baseline and 4 weeks

  2. Change in Timed Up and Go Test Time

    Functional mobility assessed using the Timed Up and Go (TUG) test, recorded as the time (in seconds) taken to rise from a chair, walk 3 meters, turn, return, and sit back down. Lower scores indicate better functional mobility.

    Time frame: Baseline and 4 weeks

  3. Change in Berg Balance Scale Score

    Overall functional balance assessed using the Berg Balance Scale (BBS), a 14-item performance-based scale with each item scored from 0 to 4, yielding a total score ranging from 0 to 56. Higher scores indicate better functional balance.

    Time frame: Baseline and 4 weeks

07

Study locations

1 site
  • Badr university in cairo
    Cairo, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

2 registry updates since Sep 25, 2026
Status
Not yet recruiting→Completed
changed Oct 13, 2026
Sites
1 site added — first site in Egypt
Show site
  • Badr university in cairo · Cairo, Egypt
Oct 13, 2026
Registered
First appeared on the registry
Sep 25, 2026
Show all 2 updates
  1. Oct 13, 2026
    Not yet recruiting→Completed
    1 site added — first site in Egypt
    Show site
    • Badr university in cairo · Cairo, Egypt
    + 3 other changes: verification date, date precision and contact details
  2. Sep 25, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07841379
Lead sponsor
Beshoy Maher Rezk Hanna
Collaborators
Badr University
Responsible party
Beshoy Maher Rezk Hanna (Physical Therapist, Badr University) — Sponsor-investigator
First posted
Sep 25, 2026
Start date
Sep 8, 2026
Primary completion
Oct 6, 2026
Completion
Oct 6, 2026
Last update
Oct 13, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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