Isometric Exercise and Endogenous Pain Inhibition

NCT ID: NCT03778476

Last Updated: 2021-02-24

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

COMPLETED

Clinical Phase

NA

Total Enrollment

43 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-05-25

Study Completion Date

2019-10-29

Brief Summary

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The purpose of this study is to identify the acute effects of isometric exercise on the inhibition of pain in individuals with fibromyalgia.

Detailed Description

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Fibromyalgia syndrome (FMS) is a chronic pain condition that is characterized by widespread pain which affects 5-8% of the general population. Past research has shown that people with FMS demonstrate enhanced pain facilitation and reduced pain inhibition in the central nervous system. Incorporating a biopsychosocial model of pain may help develop strategies to prevent the functional decline and alleviate the suffering that occurs in this population. Exercise is a mainstay of pain rehabilitation with multiple health benefits, one of which is decreasing pain; a phenomenon known as exercise induced hypoalgesia (EIH). Emerging evidence has shown that exercise decreases pain facilitation in healthy adults and in some individuals with FMS. However, it's unclear whether exercise improves pain inhibition in individuals with FMS. The purpose of this study is to investigate endogenous pain inhibition, measured by conditioned pain modulation (CPM), following isometric exercise of the quadriceps muscle in individuals with FMS. In addition, factors that might affect this response such as physical activity, body composition, and psychosocial issues will be examined. Understanding how exercise impacts pain and the contributing factors will help guide the prescription of exercise to optimize pain rehabilitation.

Conditions

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Fibromyalgia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

The two groups will participate in two sessions receiving intervention or no intervention in a randomized manner.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
The participant is masked to the hypotheses of the treatment.

Study Groups

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Isometric Exercise

Participants will perform a submaximal voluntary contraction of the quadriceps muscle to task failure.

Group Type EXPERIMENTAL

Isometric Exercise

Intervention Type OTHER

Participants will be asked to hold a submaximal voluntary contraction of the quadriceps muscle as long as they can (task failure).

Quiet Rest

Participants will sit quietly for a period of time that mimics the exercise.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Isometric Exercise

Participants will be asked to hold a submaximal voluntary contraction of the quadriceps muscle as long as they can (task failure).

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Men and women aged 18-75 diagnosed with fibromyalgia or healthy controls will be included in the study.

Exclusion Criteria

* cardiovascular disease, cancer, pregnancy, arthritis, diabetes, claustrophobia, Reynaud's disease, osteoporosis, neuropathy.
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Marquette University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Marie Hoeger Bement, PT, PhD

Role: PRINCIPAL_INVESTIGATOR

Marquette University

Ali Alsouhibani, PT, MS

Role: STUDY_DIRECTOR

Marquette University

Locations

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Marquette University

Milwaukee, Wisconsin, United States

Site Status

Countries

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United States

Other Identifiers

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HR3035

Identifier Type: -

Identifier Source: org_study_id

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