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Will the Use of Osteopathic Manipulative Treatments Help Alleviate Headache Pain

Primary Purpose

Headache

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Osteopathic Manipulative Treatment
Sham Osteopathic Manipulative Treatment
Sponsored by
Good Samaritan Hospital Medical Center, New York
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Headache focused on measuring pain, headache

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Patients will be triaged to the appropriate part of the Emergency Department in the usual fashion. A healthcare provider will evaluate the patient and if the patient's chief complaint is headache the provider will determine if they are a candidate for the study utilizing exclusion criteria for the study -

Exclusion Criteria:

Exclusion Criteria for the Study

Temperature 100.4 or greater

Healthcare provider suspects meningitis, brain abscess, encephalitis

Altered mental status

History of trauma

Cyclic vomiting

Abdominal migraines

Analgesic medication taken prior to treatment within an hour

Providing physician suspects intracranial hemorrhage

Focal deficits or other neurological abnormalities that lead providing physician to suspect a pathologic process in which osteopathic treatment would not be safe for the patient

Providing physician feels osteopathic treatment would not be safe for the patient

-

Sites / Locations

  • Good Samaritan Hospital Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Osteopathic Manipulative Treatment

Sham Osteopathic Manipulative Treatment

Arm Description

The osteopathic treatment group will have performed on them 3 standardized osteopathic manipulative treatments. If at any time the patient is unable to tolerate a treatment secondary to pain that particular study will be stopped. If the patient's nurse enters the room with medication, the study will be stopped and patient will not be included in the study. At no time will the patient's medical treatment in the emergency department be delayed to perform OMT

The sham group will receive 3 sham treatments. If at any time the patient is unable to tolerate a treatment secondary to pain that particular study will be stopped. If the patient's nurse enters the room with medication, the study will be stopped and patient will not be included in the study. At no time will the patient's medical treatment in the emergency department be delayed to perform OMT.

Outcomes

Primary Outcome Measures

Headache Pain as Measured by a VAS
The primary outcome will be the change in pain before and immediately after intervention as measured by a 100 mm visual analog scale (VAS) for pain in patients with headaches that meet the inclusion criteria.

Secondary Outcome Measures

Full Information

First Posted
September 19, 2012
Last Updated
October 10, 2012
Sponsor
Good Samaritan Hospital Medical Center, New York
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1. Study Identification

Unique Protocol Identification Number
NCT01704625
Brief Title
Will the Use of Osteopathic Manipulative Treatments Help Alleviate Headache Pain
Official Title
Will the Use of Osteopathic Manipulative Treatments on Patients With Headache in the Emergency Department Result in Decreased Pain on 100 Point Pain Scale?
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Unknown status
Study Start Date
January 2012 (undefined)
Primary Completion Date
December 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Good Samaritan Hospital Medical Center, New York

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
PURPOSE The purpose of this research is to determine whether osteopathic manipulative therapy (OMT) is a useful adjunct in evaluation and treatment of headaches. PROCEDURES If a practitioner determines that a patient has a significant headache he/she may order tests. He/ She may give the patient medications to treat the headache. The investigators will also ask permission to evaluate and treat the headache using osteopathic evaluation and Osteopathic Manipulative Treatment (OMT). The bedside evaluation and treatment will be performed by an emergency medicine resident. Osteopathic evaluation and OMT is not standard of care for this condition. The investigators also may call the patient in 7 days to see how they are doing. The investigators wish to see if emergency medicine physicians can use osteopathic evaluation and OMT to reliably treat headaches. The results of the examination and treatment will be recorded, but will not be used to change treatment or to change additional tests. The investigators wish to see whether in the future they can use OMT in certain cases instead of or in conjunction with medications. The investigators plan on asking 50 patients to participate.
Detailed Description
Will the Use of Osteopathic Manipulative Treatments on Patients with Headache in the Emergency Department Result in Decreased Pain on 100 Point Pain Scale? PROTOCOL Patients will be triaged to the appropriate part of the Emergency Department in the usual fashion. A healthcare provider will evaluate the patient and if the patient's chief complaint is headache the provider will determine if they are a candidate for the study utilizing exclusion criteria for the study TABLE 1. ___ Table 1. Exclusion Criteria for the Study Temperature 100.4 or greater Healthcare provider suspects meningitis, brain abscess, encephalitis Altered mental status History of trauma Cyclic vomiting Abdominal migraines Analgesic medication taken prior to treatment within an hour Providing physician suspects intracranial hemorrhage Focal deficits or other neurological abnormalities that lead providing physician to suspect a pathologic process in which osteopathic treatment would not be safe for the patient Providing physician feels osteopathic treatment would not be safe for the patient If patients have none of the above criteria, they may be selected for the study by the Providing Physician. The provider will ask the patient to rate their initial pain by drawing a vertical line on the 100 mm visual analog scale (VAS) on the Physician Provider Data Form. The provider will then alert an osteopathic emergency medicine resident to enroll the patient into the study. The resident will then obtain informed consent from the patient and will then take an envelope containing a piece of paper stating whether the patient is to receive the actual osteopathic treatment or if the patient will receive placebo/sham treatment. Treatment will be performed by osteopathic emergency medicine residents. Each resident has undergone training in Osteopathic Manipulative Techniques (OMT) in their respective medical schools and has fulfilled the requirements for competency in these techniques for graduation. The osteopathic treatment group will have performed on them 3 standardized osteopathic manipulative treatments. These treatments are muscle energy to the occipital area; muscle energy to the paraspinal muscles bilaterally and facilitated positional release without axial compression. If at any time the patient is unable to tolerate a treatment secondary to pain that particular study will be stopped. At no time will the patient's medical treatment in the emergency department be delayed to perform OMT.For example, if the patient's nurse enters the room with medication, the study will be stopped and patient will not be included in the study. The sham group will receive 3 sham treatments. The patient consent form and information as to whether or not the patient received osteopathic manipulative treatment will be kept in a locked file. The information will be transferred to a password-protected computer file. After the standardized treatment or sham treatment is performed, the resident will leave the patient and the providing physician will then ask the patient to draw a vertical line on the VAS to again rate their pain. The providing physician will then place the data form into the envelope that also contains the information about whether the patient received the osteopathic treatment vs. the sham treatment, without seeing the actual information. Data will then be analyzed and kept in a password-protected file.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Headache
Keywords
pain, headache

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Osteopathic Manipulative Treatment
Arm Type
Experimental
Arm Description
The osteopathic treatment group will have performed on them 3 standardized osteopathic manipulative treatments. If at any time the patient is unable to tolerate a treatment secondary to pain that particular study will be stopped. If the patient's nurse enters the room with medication, the study will be stopped and patient will not be included in the study. At no time will the patient's medical treatment in the emergency department be delayed to perform OMT
Arm Title
Sham Osteopathic Manipulative Treatment
Arm Type
Sham Comparator
Arm Description
The sham group will receive 3 sham treatments. If at any time the patient is unable to tolerate a treatment secondary to pain that particular study will be stopped. If the patient's nurse enters the room with medication, the study will be stopped and patient will not be included in the study. At no time will the patient's medical treatment in the emergency department be delayed to perform OMT.
Intervention Type
Procedure
Intervention Name(s)
Osteopathic Manipulative Treatment
Intervention Description
The investigators wish to see if emergency medicine physicians can use osteopathic evaluation and OMT to reliably treat headaches. The results of the examination and treatment will be recorded, but will not be used to change treatment or to change additional tests.
Intervention Type
Procedure
Intervention Name(s)
Sham Osteopathic Manipulative Treatment
Intervention Description
The sham group will receive 3 sham treatments.
Primary Outcome Measure Information:
Title
Headache Pain as Measured by a VAS
Description
The primary outcome will be the change in pain before and immediately after intervention as measured by a 100 mm visual analog scale (VAS) for pain in patients with headaches that meet the inclusion criteria.
Time Frame
Immediately before and after intervention (less than 30 minutes)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients will be triaged to the appropriate part of the Emergency Department in the usual fashion. A healthcare provider will evaluate the patient and if the patient's chief complaint is headache the provider will determine if they are a candidate for the study utilizing exclusion criteria for the study - Exclusion Criteria: Exclusion Criteria for the Study Temperature 100.4 or greater Healthcare provider suspects meningitis, brain abscess, encephalitis Altered mental status History of trauma Cyclic vomiting Abdominal migraines Analgesic medication taken prior to treatment within an hour Providing physician suspects intracranial hemorrhage Focal deficits or other neurological abnormalities that lead providing physician to suspect a pathologic process in which osteopathic treatment would not be safe for the patient Providing physician feels osteopathic treatment would not be safe for the patient -
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ronald Dvorkin, MD
Phone
631-376-4094
Email
ronald.dvorkin@chsli.org
First Name & Middle Initial & Last Name or Official Title & Degree
Genevieve McGerald, DO
Phone
631-376-4094
Email
genevieve.mcgerald@chsli.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Genevieve McGerald, DO
Organizational Affiliation
Good Samaritan Hospital Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Good Samaritan Hospital Medical Center
City
West Islip
State/Province
New York
ZIP/Postal Code
11795
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Genevieve McGerald, DO
Phone
631-376-4094
Email
genevieve.mcgerald@chsli.org
First Name & Middle Initial & Last Name & Degree
Ronald Dvorkin, MD
Phone
631-376-4094
Email
ronald.dvorkin@chsli.org
First Name & Middle Initial & Last Name & Degree
Genevieve McGerald, DO
First Name & Middle Initial & Last Name & Degree
Ronald Dvorkin, MD
First Name & Middle Initial & Last Name & Degree
Jacob Bair, DO
First Name & Middle Initial & Last Name & Degree
Laura Fil, DO
First Name & Middle Initial & Last Name & Degree
Donie Marie Sergerivas, DO
First Name & Middle Initial & Last Name & Degree
Shannon Weinstein, DO

12. IPD Sharing Statement

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Will the Use of Osteopathic Manipulative Treatments Help Alleviate Headache Pain

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