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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06108323
Other study ID # 2023-FIS-2731776-1
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 27, 2023
Est. completion date December 2024

Study information

Verified date May 2024
Source University of Valencia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to learn about the effects who would add mental practice based on action observation to a therapeutic exercise program in young mild smokers. The main question it aims to answer is whether the observation of actions prior to the implementation of a therapeutic exercise session improves the response to it on respiratory, strength and muscle function variables. Participants will be assigned to one of 2 study groups: G1) Therapeutic exercise plus action observation training (n=20) G2) Therapeutic exercise plus sham action observation training (n=20)


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 34
Est. completion date December 2024
Est. primary completion date April 28, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - >18 years old - Had a pack per year index of <5 (mild smoking index). Exclusion Criteria: Those who presented: - a respiratory pathology, - cardiac, systematic, or metabolic disease, - history of recent surgery, - vertebral fracture, - or osteoarticular disorders of the spine area.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Theapeutic exercise plus action observation training
Participants make an observation of actions related to the training they are going to perform. Subsequently, they perform the therapeutic exercise session.
Therapeutic exercise plus sham observation training
Participants make a sham observation. Subsequently, they perform the therapeutic exercise session.

Locations

Country Name City State
Spain Universitat de Valencia Valencia

Sponsors (1)

Lead Sponsor Collaborator
University of Valencia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Respiratory strength Maximal respiratory pressures (in H2O centimeters) Preintervention and inmediately after the intervention
Secondary Respiratory function parameters Spirometric parameters (in liters/second) Preintervention and inmediately after the intervention
Secondary Physical function 5 times sit-to-stand test (in seconds) Preintervention and inmediately after the intervention
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