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A Novel Ballet-inspired Low-impact At-home Workout Programme for Adults with Stroke

Feasibility of a Novel Ballet-inspired Low-impact At-home Workout Programme to Improve Balance, Gait and Memory in Adults with Stroke: a Mixed Methods Exploratory Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04460794
Enrollment
32
Registered
2020-07-08
Start date
2020-08-03
Completion date
2023-12-31
Last updated
2024-11-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Balance; Distorted, Gait, Unsteady, Memory Impairment, Stroke

Brief summary

To explore the feasibility of a novel ballet-inspired low-impact at-home workout programme for community-dwelling stroke survivors in Hong Kong.

Detailed description

A mixed methods exploratory study incorporating a randomised controlled trial (RCT) and qualitative evaluation will be conducted. A total of 40 stroke participants will be recruited from two acute public hospitals. Participants will be randomly assigned to receive the interention and usual care, or usual care only. Data will be collected in multiple forms: recruitment/retention rates, adherence to the intervention, journals, field notes, verbal feedback, audio records, semi-structured interviews, and questionnaires on outcomes (balance, confidence in balance, gait, walking endurance). This study is the first of its kind in Hong Kong. Findings will address the cross-cultural applicability of dance interventions and lay the groundwork for examination in a larger-RCT about its effects on survivors' balance, gait and memory.

Interventions

BEHAVIORALBallet-inspired workouts

8 weeks, delivered by volunteers with a self-directed resource package

OTHERUsual care

Usual care and general recommendations on basic stretching and leg exercises for stroke survivors

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. aged 18 years or above 2. clinically diagnosed with a first-ever ischaemic/ haemorrhagic stroke 3. living in home settings 4. mild-moderate lower limb paresis with a modified Functional Ambulation Classification (MFAC) of III (Dependent walker) or above 5. a Montreal Cognitive Assessment (MoCA) score\>20 6. able to follow three-step directions 7. able to communicate in Cantonese and read Traditional Chinese 8. their hearing and/or visual disturbances corrected by hearing aids and/or glasses 9. consent to participate in the study

Exclusion criteria

1. diagnosed with transcient ischaemic attack, subdural or epidural haemorrhage 2. experienced cerebrovascular events due to tumours or head trauma 3. have pre-existing neurological, cardiovascular or orthopaedic conditions that contradict participation in dancing such as shoulder dislocation, myocardial infarction, seizures or acutes illness 4. mental condition such as depression, schizophrenia or personality disorder 5. incomprehensible speech 6. severe hearing and/or visual disturbance

Design outcomes

Primary

MeasureTime frameDescription
Change in the participants' level of balanceChange from baseline to immediately after completion of the intervention (over 8 weeks)The 14-item Mini-Balance Evaluation Systems Test (Mini-BESTest) will be used. It measures four domains: anticipatory postural adjustments, reactive postural control, sensory orientation, dynamic gait. Items are rated on a 3-level scale (0=Severe, 1=Moderate, 2=Normal). Summed total score=0-28 (higher scores representing better balance ability). Cronbach alpha=0.89-0.94.

Secondary

MeasureTime frameDescription
Change in the participants' level of balance confidenceChange from baseline to immediately after completion of the intervention (over 8 weeks)The 16-item Activities-specific Balance Confidence Scale (Chinese version) will be adopted. Participants will rate their confidence in balance associated with performing 16 daily functional activities from 0% (absolutely no confidence) to 100% (fully confident). Summed total score=0-100% (higher scores denotes higher confidence). Cronbach alpha=0.97.
Change in the participants' level of gaitChange from baseline to immediately after completion of the intervention (over 8 weeks)The 31-item Gait Assessment and Intervention tool (G.A.I.T.) will be used to measure gait: upper extremity and trunk movement control; trunk and lower extremity (stance phase); trunk and lower extremity (swing phase). Each item is scored from 0 (normal) to 3, with gradients of variation from normal (Total score: 0 (normal gait) to 62 (greatest extent of gait deviations)). It has good intra-rater and interrater reliability.
Change in participants' level of walking enduranceChange from baseline to immediately after completion of the intervention (over 8 weeks)The 6-Minute Walk Test (MWT) will be performed in accordance with American Thoracic Society guidelines. The distance walked, the time stopped and reason(s) for stopping prematurely will be recorded. 6MWT, 12MWT, and self-paced gait speed were all significantly highly correlated (r\>0.90).
Change in participants' level of memoryChange from baseline to immediately after completion of the intervention (over 8 weeks)The 11-item Rivermead Behavioural Memory Test - Third Version (Chinese version) will be used. For each task, scores range from 0-2 (2-points=normal; 1-point=intermediate; 0-point=error). Total score=0-254. It demonstrated a high inter-rater reliability. Correlation between performance on parallel forms=0.67-0.84.

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026