The Effects Of Equal Breathing On Pain Pressure Thresholds

NCT ID: NCT03353142

Last Updated: 2018-06-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-02-01

Study Completion Date

2019-02-01

Brief Summary

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Recent research has found that there is moderate evidence for the use of breathing exercises for treating chronic, non-specific low back pain. Researchers have found that there were significant improvements in pain and quality of life in those suffering with low back pain who completed a breathing program intervention. Researchers also found that healthy individuals had higher pain thresholds and tolerance following deep and slow breathing exercises.

There are numerous formats of breathing interventions, some interventions that have been used with individuals with chronic, non-specific low back pain include: deep breathing, yoga breathing, resisted inspiration, and breathe holding. There is moderate evidence to suggest the use of these interventions for managing chronic low back pain Another common breathing format is Equal-Ratio Breathing. This format requires an individual to inhale and exhale with the same duration while gradually increasing the duration of both. This breathing format can be easier for patients to perform given the simplicity of the equal inhalation to exhalation ratio.

This research is being done because Equal-Ratio Breathing has yet to be studied in individuals with chronic low back pain.

Detailed Description

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Conditions

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Chronic Low Back Pain

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Consecutive participants meeting eligibility criteria will be enrolled
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Equal Breathing

Group Type EXPERIMENTAL

Equal Breathing

Intervention Type OTHER

* Blood pressure recorded at baseline, immediately pre- and post-trial
* Maximum Tolerable Breathing Ratio: Test run to determine the maximum tolerable time for inhalation and exhalation.
* PRESSURE TOLERANCE: Pressure algometer device used to determine pain pressure tolerance. It will be applied to the first dorsal interosseous and deltoid, and pain pressure tolerance will be measured and recorded. Pressure will be applied at 1kg per second until the patient indicates that the pressure has become painful. Pain pressure tolerance will be performed 3 times at each anatomical location and an average will be determined for each location.
* TRIAL: Participants will begin 5 minutes of Equal Breathing at their maximum tolerable equal breathing ratio that was previously determined. Immediately after 5 minutes of breathing, the pain pressure tolerance will be measured using pressure algometry

Interventions

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Equal Breathing

* Blood pressure recorded at baseline, immediately pre- and post-trial
* Maximum Tolerable Breathing Ratio: Test run to determine the maximum tolerable time for inhalation and exhalation.
* PRESSURE TOLERANCE: Pressure algometer device used to determine pain pressure tolerance. It will be applied to the first dorsal interosseous and deltoid, and pain pressure tolerance will be measured and recorded. Pressure will be applied at 1kg per second until the patient indicates that the pressure has become painful. Pain pressure tolerance will be performed 3 times at each anatomical location and an average will be determined for each location.
* TRIAL: Participants will begin 5 minutes of Equal Breathing at their maximum tolerable equal breathing ratio that was previously determined. Immediately after 5 minutes of breathing, the pain pressure tolerance will be measured using pressure algometry

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Aged ≥ 18
* Chronic low back pain
* OHIP patient

Exclusion Criteria

* Peripheral pain
* Peripheral neuropathy
* Chronic regional pain syndrome
* Alpha and Beta blocker medication use
* Patient does not wish to participate
* Completed or participated in a psychoeducational program at the clinic
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hamilton Health Sciences Corporation

OTHER

Sponsor Role lead

Responsible Party

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Gurpreet Palak

Physician - Fellow

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Michael G. DeGroote Pain Clinic, Hamilton Health Sciences

Hamilton, Ontario, Canada

Site Status RECRUITING

Countries

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Canada

Central Contacts

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Gurpreet Palak

Role: CONTACT

905-521-2100

Lisa Patterson, BA

Role: CONTACT

905-521-2100 ext. 74279

Facility Contacts

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Lisa Patterson, B.A.

Role: primary

905-521-2100 ext. 74279

Other Identifiers

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MGD-004-20171016

Identifier Type: -

Identifier Source: org_study_id

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