- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05411536
Attentional Focus Instructions and Conscious Movement Processing in Older Adults
The Effects of Attentional Focus Instructions on Real-time Conscious Movement Processing While Walking in a Challenging Environment for Older Adults at Risk of Falling in Hong Kong: Implications for Rehabilitation
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
-
Hong Kong, China
- The Hong Kong Polytechnic University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- age 65 or above;
- able to walk independently indoor for at least 20 metres without a walking aid.
Exclusion Criteria:
- a total score of less than 24 on the MMSE-C (Chiu et al., 1994; Folstein et al., 1975);
- the presence of any untreated cerebral vascular disease, Parkinson's disease, or any other major neurological deficit;
- the presence of an unstable medical condition affecting safety while walking ;
- a history of a major fall incident within the last year;
- a static visual acuity poorer than 20/40 vision (assessed using the Tumbling E eye chart).
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
high reinvestor group (HRG)
The participants were divided into two groups, the high reinvestor group (HRG) and the low reinvestor group (LRG), using the conventional median split of their scores on the MSRS-C (Chu & Wong, 2019; Mak et al., 2020).
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All participants will complete a series of walking trials. They will first be requested to perform three practice walks followed by three walking trials on a 7.4m straight level-ground firm walkway (GW) and the other three walking trials on a 7.4m straight foam walkway (FW) in a randomised order. The dimension of the foam walkway in the FW will be 8m (length), 0.8m (width), and 0.3m (height). The starting and finishing lines of the FW will be positioned at 0.3m from each side of the FW's edges. Thus, the lengths of the FW and the GW will be identical (i.e., 7.4m). Participants will be asked to walk 7.4m and stop for each walking trial. After a 10-minute rest break, participants will perform nine walking trials on the GW and the other nine walking trials on the FW, including three repetitions of three different attentional focus instructions (external focus [EF], internal focus [IF], and no specific focus [NF]) in the GW and FW in a randomised order. |
|
low reinvestor group (LRG)
The participants were divided into two groups, the high reinvestor group (HRG) and the low reinvestor group (LRG), using the conventional median split of their scores on the MSRS-C (Chu & Wong, 2019; Mak et al., 2020).
|
All participants will complete a series of walking trials. They will first be requested to perform three practice walks followed by three walking trials on a 7.4m straight level-ground firm walkway (GW) and the other three walking trials on a 7.4m straight foam walkway (FW) in a randomised order. The dimension of the foam walkway in the FW will be 8m (length), 0.8m (width), and 0.3m (height). The starting and finishing lines of the FW will be positioned at 0.3m from each side of the FW's edges. Thus, the lengths of the FW and the GW will be identical (i.e., 7.4m). Participants will be asked to walk 7.4m and stop for each walking trial. After a 10-minute rest break, participants will perform nine walking trials on the GW and the other nine walking trials on the FW, including three repetitions of three different attentional focus instructions (external focus [EF], internal focus [IF], and no specific focus [NF]) in the GW and FW in a randomised order. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle efficiency
Time Frame: Day 0
|
It will be measured by the surface electromyography (EMG).
|
Day 0
|
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Real-time (state) conscious movement processing propensity
Time Frame: Day 0
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It will be measured by the Alpha2 EEG T3-Fz coherence.
|
Day 0
|
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Gait speed
Time Frame: Day 0
|
It will be measured by the 3-D motion-capture system in the unit of meter per second (m/s).
|
Day 0
|
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Body sway
Time Frame: Day 0
|
It will be measured by the 3-D motion-capture system in the unit of millimeter (mm).
|
Day 0
|
|
Stride length
Time Frame: Day 0
|
It will be measured by the 3-D motion-capture system in the unit of meter (m).
|
Day 0
|
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Stride-to-stride variability
Time Frame: Day 0
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It will be measured by the 3-D motion-capture system by the coefficients of variation (CV).
|
Day 0
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance ability
Time Frame: Day 0
|
It will be measured by the Berg Balance Scale.
The minimum value of the scale is 0 and the maximum value is 56.
Higher score represents better balance ability.
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Day 0
|
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Walking ability
Time Frame: Day 0
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It will be measured by the Timed 'Up & Go' tests.
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Day 0
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Fear of falling
Time Frame: Day 0
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It will be measured by the Chinese version of the Falls Efficacy Scale International.
The minimum value of the scale is 16 and the maximum value is 64.
Higher score represents higher fear of falling.
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Day 0
|
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Trait conscious movement processing propensity
Time Frame: Day 0
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It will be measured by the Chinese version of the Movement-Specific Reinvestment Scale.
The minimum value of the scale is 10 and the maximum value is 60.
Higher score represents higher trait conscious movement processing propensity.
|
Day 0
|
Collaborators and Investigators
Investigators
- Principal Investigator: Thomson Wong, PhD, The Hong Kong Polytechnic University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 15601021
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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