CClinicalTrials.gg
CompletedNCT03149458DanceStudioUpdated Sep 18, 2026

Dance Workshop on Balance of Hemiparetic Patients

An interventional study of dance and control in Hemiparesis, sponsored by Centre d'Investigation Clinique et Technologique 805. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-18.

Sponsored by Centre d'Investigation Clinique et Technologique 805 · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
31
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The majority of hemiparetic patients have balance disorders, which impact independence in daily living activities and walking. Conventional techniques used in rehabilitation improve balance but have shown no effects on dynamic balance required during walking. Recently dance is proposed to improve dynamic balance in older people and people with Parkinson's disease. Although many studies showed that dance is an effective activity to improve balance in these people, it has never been assessed in hemiparetic patients (except a case report). The aim of this study is to show that a dance program improves the balance of hemiparetic patients, compared to a control group. This randomized controlled study aims to include 40 hemiparetic patients who will perform a dance program (experimental group) or a upper-limb rehabilitation program (control group) for 8 one-hour sessions.

Read the detailed description

Randomized controlled study aims to include 40 hemiparetic patients who will perform a dance program (experimental group) or a upper-limb rehabilitation program (control group) for 8 one-hour sessions. These activities are carried out in the form of a workshop and are already proposed in common practice in the service. They are carried out by the physiotherapists of the service. Patients are assigned in one of two study groups. It is specified that they will be able to carry out the program of the opposing group at the end of the study in order to limit the "disappointment" effect. The evaluations will be carried out at 4 and 8 weeks and will mainly rely on data of balance, function, quality of life and satisfaction

02

Conditions studied

  • Hemiparesis

Browse trials for

Keywords

  • stroke
  • balance
  • dance
03

In context

Paresis

519 studies on the registry are indexed under Paresis; 111 are open to participants now.

This study's enrollment of 31 is below the median of 36 across 448 interventional studies indexed under Paresis.

Browse Paresis studies →

Lead sponsor

Centre d'Investigation Clinique et Technologique 805 is the lead sponsor of 74 studies on the registry; 2 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient who signed the consent letter
  • Male or female adults age ≥ 18 years,
  • Hemiparetic patient
  • Patient with balance disorders, able to walk alone and perform a U-turn, with or without technical assistance.

Exclusion criteria

Exclusion Criteria:

  • Bilateral brain lesions, cerebellar syndrome
  • Other pathology or impairment that may interfere with the study such as visual, cardiovascular or other uncontrolled medical conditions
  • Patient who underwent surgery of the musculoskeletal system in The 6 months prior to inclusion
  • Major cognitive disorders not allowing the dance activity or the passing of evaluations
  • Behavioral disorders not allowing group workshops
  • Pregnant woman, breastfeeding
  • Non-affiliation to a social security scheme (beneficiary or beneficiary)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
31 participants (actual)

Study arms

  • Experimental
    Dance group

    dance program for 8 one-hour sessions.

    Other: dance

  • Active comparator
    control group

    upper limb rehabilitation for 8 one-hour sessions.

    Other: control

Interventions

  • Otherdance

    dance program

  • Othercontrol

    upper limb rehabilitation

06

What researchers measure

Primary outcomes

  1. Timed up and Go

    get up, walk 3m, turn around and return sit down

    Time frame: 5min

Secondary outcomes

  1. Berg Balance Scale

    clinical scale assessing balance. 14-item scale designed to measure balance of the older adult in a clinical setting. Scoring: A five-point scale, ranging from 0-4. "0" indicates the lowest level of function and "4" the highest level of function. Total Score = 56

    Time frame: 10min

07

Study locations

1 site
  • Raymond Poincaré Hospital- PMR Unit - Netter
    Garches, 92380, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03149458
Lead sponsor
Centre d'Investigation Clinique et Technologique 805
Collaborators
Fondation Garches
Responsible party
Sponsor
First posted
May 11, 2017
Start date
Mar 15, 2017
Primary completion
Jul 20, 2022
Completion
Jul 8, 2025
Last update
Sep 18, 2026

Study contacts

François GENET, PhD
principal investigator · Centre d'Investigation Clinique et Technologique 805

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 Sep 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion