Skip to main content
Clinical Trials/NCT04460794
NCT04460794CompletedNot Applicable

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

Chinese University of Hong Kong1 site in 1 country32 target enrollmentStarted: August 3, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
32
Locations
1
Primary Endpoint
Change in the participants' level of balance

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

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

Exclusion Criteria

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

Outcomes

Primary Outcomes

Change in the participants' level of balance

Time Frame: Change 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 Outcomes

  • Change in the participants' level of balance confidence(Change from baseline to immediately after completion of the intervention (over 8 weeks))
  • Change in the participants' level of gait(Change from baseline to immediately after completion of the intervention (over 8 weeks))
  • Change in participants' level of memory(Change from baseline to immediately after completion of the intervention (over 8 weeks))
  • Change in participants' level of walking endurance(Change from baseline to immediately after completion of the intervention (over 8 weeks))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Suzanne HS Lo

Assistant Professor

Chinese University of Hong Kong

Study Sites (1)

Loading locations...

Similar Trials