NCT07578493

Brief Summary

Hemiparesis following a stroke is associated with persistent deficits in postural control, balance, and social participation, especially in the chronic phase. Dance therapy, as a multisensory intervention based on movement, music, and body expression, could promote sensorimotor integration and improve postural stability, complementing conventional physiotherapy. The primary objective of this pilot study is to evaluate the effect of a therapeutic dance program on postural control in individuals with chronic hemiparesis. A secondary objective is to analyze changes in functional balance and gait, as well as subjective satisfaction with the therapy. A controlled study with two parallel groups will be conducted. Sixteen participants with chronic hemiparesis will be recruited (n=8 experimental group; n=8 control group). Both groups will receive standard physiotherapy, but the experimental group will also receive an 8-week therapeutic dance program, with one 30-minute session per week to complement their usual therapy. Pre- and post-intervention assessments will be performed. ThThe experimental group is expected to show a significantly greater improvement in posturographic and clinical parameters compared to the control group. The results could support the implementation of dance therapy as a complementary intervention in community neurorehabilitation programs.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
7mo left

Started May 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress4%
May 2026Nov 2026

First Submitted

Initial submission to the registry

April 28, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

May 11, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

May 15, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2026

Last Updated

May 11, 2026

Status Verified

May 1, 2026

Enrollment Period

6 months

First QC Date

April 28, 2026

Last Update Submit

May 5, 2026

Conditions

Keywords

Dance TherapyStrokePostural balanceGaitPhysical Therapy Modalities

Outcome Measures

Primary Outcomes (2)

  • Static and dynamic postural control

    The oscillation of the Center of Pressure will be recorded in millimeters during the static position (Romberg test, hold the position with feet together with eyes open and eyes closed for 52 seconds) and walking at your preferred speed.

    From enrollment to the end of treatment at 8 weeks

  • Load distribution during gait

    The percentage (%) of load on each leg will be recorded during walking at your preferred speed.

    From enrollment to the end of treatment at 8 weeks

Secondary Outcomes (2)

  • Satisfaction with the activity

    After completing the 8-week intervention

  • Adherence to treatment

    After completing the 8-week intervention

Study Arms (2)

Dance therapy group

EXPERIMENTAL
Other: Dance therapyOther: Regular physiotherapy

Conventional treatment group

ACTIVE COMPARATOR
Other: Regular physiotherapy

Interventions

The experimental group will participate in an 8-week therapeutic dance program, with one 30-minute session per week, as a complement to their regular physiotherapy. Each session will integrate: • Bilateral and diagonal PNF patterns adapted to the affected side of the body. • Rhythmic movement guided by moderate-tempo music. • Exercises focused on postural symmetry and weight transfer. • Explicit and implicit motor learning strategies. The rhythmic components will be selected to optimize audio-motor synchronization, while the PNF patterns will aim to maximize sensorimotor activation and proximal stability. The intervention will be adaptable and progressive according to the patient's clinical response.

Dance therapy group

All participants, including those in the control group, will receive standard physiotherapy provided by their primary care center, focused on functional maintenance, mobility, and strengthening, without dance or rhythmic PNF components. They will receive two 40-minute sessions per week, individualized and adapted to their functional status.

Conventional treatment groupDance therapy group

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Chronic hemiparesis (≥ 6 months post-stroke).
  • Ability to maintain independent standing or with minimal assistance.
  • Clinical stability to perform moderate physical exercise.
  • Sufficient understanding to follow simple instructions.

You may not qualify if:

  • Severe aphasia or other cognitive disorders that limit comprehension.
  • Behavioral disorders that hinder group participation.
  • Severe musculoskeletal disorders or concomitant neurological conditions.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Salamanca

Salamanca, Salamanca, 37008, Spain

Location

MeSH Terms

Conditions

Stroke

Interventions

Dance Therapy

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

Sensory Art TherapiesComplementary TherapiesTherapeuticsRehabilitationAftercareContinuity of Patient CarePatient CareExercise Movement TechniquesPhysical Therapy ModalitiesPsychotherapyBehavioral Disciplines and Activities

Central Study Contacts

Fatima Perez-Robledo, Dr.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr.

Study Record Dates

First Submitted

April 28, 2026

First Posted

May 11, 2026

Study Start

May 15, 2026

Primary Completion (Estimated)

October 30, 2026

Study Completion (Estimated)

November 30, 2026

Last Updated

May 11, 2026

Record last verified: 2026-05

Locations