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Recruiting NCT05924113

A Study of Latin Dance for Post- Lung Transplant

No phase Interventional Lung Transplant Well-Being, Psychological

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Latin Dance.
Who it may be relevant to
Registry conditions: Lung Transplant, Well-Being, Psychological. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Efficacy of Latin Dance for Promoting Wellbeing in Post Lung Transplant Recipients as Measured by Several Functional Measures, in the Outpatient Setting

Overview

The purpose of this research study is to see if participating in Latin dance for 12 sessions can improve wellbeing in several areas including balance, fear of movement, anxiety, depression and spirometry.

Interventions

  • Behavioral Latin Dance
    Latin dance sessions that include a warm-up routine with music, two choreographed dances, and a cooldown routine with music.

Primary outcome measures

  • Change in anxiety [Time frame: Baseline, 12 weeks]
  • Change in depression [Time frame: Baseline, 12 weeks]
  • Change in Tampa Kinesophobia Scale [Time frame: Baseline, 12 weeks]
Secondary outcome measures (2)
  • Change in gait [Time frame: Baseline, 12 weeks]
  • Change in Forced Expiratory Volume in one second (FEV1) [Time frame: Baseline, 12 weeks]

Eligibility criteria

Inclusion criteria

\- Ambulatory with or without assisting devices (not on supplemental oxygen is not exclusionary), who have completed outpatient cardiopulmonary rehab and good pain control.

Exclusion criteria

\- Tracheostomy, Hemodialysis, gastro-jejunal tubes, nasogastric tubes, wound vacs, chest tube, high levels of oxygen supplementation (mask vs nasal canula), recent falls.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Supportive care

Study locations

United States · 1 center
  • Mayo Clinic Florida — Jacksonville

Identifiers

NCT: NCT05924113 · 23-001508

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗