Attentional Focus Instructions and Conscious Movement Processing in Older Adults

Sponsor
The Hong Kong Polytechnic University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05411536
Collaborator
(none)
106
1
23.5
4.5

Study Details

Study Description

Brief Summary

This study aims to provide a novel scientific contribution through addressing critical knowledge gaps, examining the effects of attentional focus instructions on real-time (state) conscious movement processing propensity, gait parameters, and muscle efficiency in older adults in Hong Kong at risk of falling while walking in a challenging environment. The study results could update our scientific understanding of the mechanisms of conscious movement processing and the interventional effects of attentional focus instructions in older adults. It could ultimately enhance the methodology used for developing the most appropriate psychomotor gait re-education intervention in rehabilitation and provide clear guidelines on the exact attentional focus training that older adults require. Further, it could mitigate the effect of conscious movement processing and risk of falling in older adults.

Condition or Disease Intervention/Treatment Phase
  • Other: Walking trials

Study Design

Study Type:
Observational
Anticipated Enrollment :
106 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
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
Actual Study Start Date :
Jul 15, 2022
Anticipated Primary Completion Date :
Jun 30, 2024
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm 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).

Other: Walking trials
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).

Other: Walking trials
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.

Outcome Measures

Primary Outcome Measures

  1. Real-time (state) conscious movement processing propensity [Day 0]

    It will be measured by the Alpha2 EEG T3-Fz coherence.

  2. Gait speed [Day 0]

    It will be measured by the 3-D motion-capture system in the unit of meter per second (m/s).

  3. Body sway [Day 0]

    It will be measured by the 3-D motion-capture system in the unit of millimeter (mm).

  4. Stride length [Day 0]

    It will be measured by the 3-D motion-capture system in the unit of meter (m).

  5. Stride-to-stride variability [Day 0]

    It will be measured by the 3-D motion-capture system by the coefficients of variation (CV).

  6. Muscle efficiency [Day 0]

    It will be measured by the surface electromyography (EMG).

Secondary Outcome Measures

  1. Walking ability [Day 0]

    It will be measured by the Timed 'Up & Go' tests.

  2. Balance ability [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.

  3. Fear of falling [Day 0]

    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.

  4. Trait conscious movement processing propensity [Day 0]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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).

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Hong Kong Polytechnic University Hong Kong China

Sponsors and Collaborators

  • The Hong Kong Polytechnic University

Investigators

  • Principal Investigator: Thomson Wong, PhD, The Hong Kong Polytechnic University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
The Hong Kong Polytechnic University
ClinicalTrials.gov Identifier:
NCT05411536
Other Study ID Numbers:
  • 15601021
First Posted:
Jun 9, 2022
Last Update Posted:
Aug 9, 2022
Last Verified:
Jun 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by The Hong Kong Polytechnic University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 9, 2022