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Effect of Thoracic Spine Mobilization on Sympathetic Nervous Systems

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Bern University of Applied Sciences

Status

Completed

Conditions

Erythema

Treatments

Procedure: Mobilization anterior
Procedure: Mobilization posterior

Study type

Observational

Funder types

Other

Identifiers

NCT02832141
Mobilization Thoracic Spine

Details and patient eligibility

About

This pilot study aims to i) represents the feasibility of the study design and ii) to point out acute effects of thoracic spine mobilization on skin-blood flow, erythema and the sympathetic nervous system.

Enrollment

14 patients

Sex

All

Ages

20 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age 20 - 30 years
  • healthy persons

Exclusion criteria

  • current pain
  • blood pressure medications
  • osteoporosis
  • cardiac or neurological symptoms
  • pregnancy
  • thromobosis

Trial design

14 participants in 2 patient groups

Group A
Description:
Group A: immediate effects: T0, Grade 3 central thoracic mobilization from posterior-to-anterior on thoracic vertebrae from T5 to T12, immediate (T1), after 2 (T2), 4 (T3), 6 (T4), 8 (T5) and 10 (T6) minutes, 1 days wash-out period; T7, a grade 3 central thoracic mobilization from anterior-to-posterior on all thoracic vertebrae, immediate T8, after 2 (T9), 4 (T10), 6 (T11), 8 (T12) and 10 (T13) minutes.
Treatment:
Procedure: Mobilization posterior
Procedure: Mobilization anterior
Group B
Description:
Group B: immediate effects: T0, 3 central thoracic mobilization from anterior-to-posterior on thoracic vertebrae from T5 to T12, immediate (T1), after 2 (T2), 4 (T3), 6 (T4), 8 (T5) and 10 (T6) minutes, 1 days wash-out period; T7, a grade 3-4 central thoracic mobilization from posterior-to-anterior on all thoracic vertebrae, immediate T8, after 2 (T9), 4 (T10), 6 (T11), 8 (T12) and 10 (T13) minutes.
Treatment:
Procedure: Mobilization posterior
Procedure: Mobilization anterior

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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