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Effect of Thoracic Spine Mobilization on Sympathetic Nervous Systems

Effect of Thoracic Spine Mobilization on Skin-blood Flow, Erythema and Sympathetic Nervous Systems

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02832141
Enrollment
14
Registered
2016-07-14
Start date
2016-05-31
Completion date
2018-12-31
Last updated
2019-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erythema

Keywords

Skin blood flow, Skin redness, Sympathetic nervous system, Regional Blood Flow

Brief summary

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.

Interventions

PROCEDUREMobilization posterior

Participant in sitting position. Central thoracic mobilization from anteriors-to-posterior.

PROCEDUREMobilization anterior

Participant in prone position. Central thoracic mobilization from posterior-to-anterior.

Sponsors

Bern University of Applied Sciences
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* age 20 - 30 years * healthy persons

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Feasibility: Adherence of recruited participantsEvery 4 weeks up to 2 yearsDefined as the number of drop-outs and presence of participants which invited. Measurement unit: number
Feasibility of the investigating procedureEvery 4 weeks up to 2 yearsMeasured the burden of testing procedure. Measurement units = number and percentage
Feasibility of the mobilization intervention from posterior-to-anterior on thoracic vertebraeEvery 4 weeks up to 2 yearsMeasured adverse effects as pain and harm results to participants. Measurement units = number and percentage
Feasibility of the mobilization intervention from anterior-to-posterior on thoracic vertebraeEvery 4 weeks up to 2 yearsMeasured as adverse effects as pain and harm results to participants. Measurement units = number and percentage.

Secondary

MeasureTime frameDescription
Rate of skin-blood flow variationChange from baseline imediately after, 2, 4, 6, 8 and 10 minutes after the interventionLaser doppler imaging is used for measuring microcirculatory changes. Measurement units: perfusion unit
Rate of heart rate variability (HRV)Change from baseline imediately after, 2, 4, 6, 8 and 10 minutes after the interventionHRV is measured as the variations of the time interval between two consecutive cardiac beats registered by means Polar watch RS800 is used to measures (HRV). Measurement unit: High frequency-band (HF-Band) and Low frequency-band (LF-Band)
Rate of erythemaChange from baseline imediately after, 2, 4, 6, 8 and 10 minutes after the interventionTristimulus surface colorimetry is used for measuring erythema. Measurement units: Erythema index
Rate of systolic blood pressure value (mmHg)Change from baseline imediately after, 2, 4, 6, 8 and 10 minutes after the interventionOmron MIT Elite Plus is used for measuring systolic blood flow. iMeasurement units: mmHg (millimeter of mercury)
Rate of diastolic blood pressure value (mmHg) changesChange from baseline imediately after, 2, 4, 6, 8 and 10 minutes after the interventionOmron MIT Elite Plus is used for measuring diastolic blood pressureMeasurement units: mmHg (millimeter of mercury)
Rate of heartbeat frequencyChange from baseline imediately after, 2, 4, 6, 8 and 10 minutes after the interventionPolar watch RS800 is used for measuring heartbeat frequency. Measurement units: beat per minute (bpm)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026