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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02464475
Other study ID # InterOST
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2015
Est. completion date December 2017

Study information

Verified date March 2019
Source Come Collaboration
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Recent evidence suggested that the anterior insula cortex seems to be the main site of interoception. Several studies showed an association between change in insula function and interoception, bodily perception and consciousness in subjects with chronic pain. Although osteopathic research has been demonstrated to be effective in reducing pain, studies exploring the effect of osteopathy on interoception are lacking. Therefore, the aim of the present study is to explore the extent to which osteopathic treatment could modify interoception parameters both measuring brain functional connectivity and clinical questionnaires.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 2017
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender All
Age group 30 Years to 50 Years
Eligibility Inclusion Criteria:

- chronic low back pain

- written informed consent signed

Exclusion Criteria:

- congenital disease

- acute pain

- subject below 30 and above 50

- co-morbidities associated with low back pain

- surgical patients

- cardio-vascular, respiratory, gastro-enteric disease

- obese subjects

- diabetics

- dizziness

- subjects into pharmacological prophylaxis

- drug addicted subjects

- subjects undergoing physiotherapy

- subjects with experience in osteopathic treatment

Study Design


Related Conditions & MeSH terms


Intervention

Other:
osteopathic manipulative treatment

sham osteopathic treatment


Locations

Country Name City State
Italy University of Chieti-Pescara Chieti

Sponsors (2)

Lead Sponsor Collaborator
Come Collaboration University of Chieti

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary functional connectivity on right anterior insula cortex before-after change in fMRI values 4 weeks
Secondary differences on salience network activities report any change between study and control group on pattern activation of salience network 4 weeks
Secondary acute changes on salience network voxel differences 2 hours
Secondary resting state network differences between groups voxel differences 4 weeks
Secondary DTI changes between groups differences in DTI parameters and indexes 4 weeks
Secondary changes in GABA concentration amount of GABA in the given voxel 4 weeks
Secondary changes in quality of life SF-36v2 self-reported questionnaire 4 weeks
Secondary changes in perception of pain McGill self-reported questionnaire 4 weeks
Secondary changes in disability Oswestry disability questionnaire 4 weeks
Secondary changes in depression symptoms Beck Depression Inventory questionnaire 4 weeks
Secondary changes in anxiety symptoms Hospital Anxiety and Depression Scale questionnaire 4 weeks
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