UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000017457
Receipt number R000020236
Scientific Title Immediate effects of cervical spine manipulation on upper extremity ergometer performance to muscle failure amongst asymptomatic participants
Date of disclosure of the study information 2015/05/08
Last modified on 2015/05/08 00:27:37

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Basic information

Public title

Immediate effects of cervical spine manipulation on upper extremity ergometer performance to muscle failure amongst asymptomatic participants

Acronym

upper limb endurance and manipulation

Scientific Title

Immediate effects of cervical spine manipulation on upper extremity ergometer performance to muscle failure amongst asymptomatic participants

Scientific Title:Acronym

upper limb endurance and manipulation

Region

North America


Condition

Condition

Cervical spine manipulation

Classification by specialty

Medicine in general Rehabilitation medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Researchers measured how cervical spine manipulation impacted upper extremity exercise performance.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Exercise time to exhaustion, exercise heart rate, blood lactate, post 1-min Rating of Perceived Exertion (RPE), and post 5-min RPE were recorded during each session.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Randomized

Randomization unit


Blinding

Open -but assessor(s) are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Cervical spine manipulation

Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit

55 years-old >=

Gender

Male and Female

Key inclusion criteria

no contraindication to cervical SMT,
between the ages of 20-55 years of age,
answer no to all sections of the Physical
Activity Readiness Questionnaire,
they provided their informed written consent

Key exclusion criteria

unstable fractures, neck surgery, multiple myeloma, osteopenia, primary bone tumor
, Paget's disease
, spinal cord tumor
, rheumatoid arthritis
, psoriatic arthritis
, ankylosing spondylitis
, Reiter's syndrome
, unstable bleeding disorders
, receiving cervical SMT in the past 2 days
, report shoulder, elbow, wrist, or
hand injury
, body pain rated greater than a 3 on
a 1-10 Numeric Rating Scale

Target sample size

46


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name John Ward, DC, MA, MS

Organization

Texas Chiropractic College

Division name

Research

Zip code


Address

5912 Spencer Highway, Pasadena, TX 77505

TEL

2819985704

Email

jward@txchiro.edu


Public contact

Name of contact person

1st name
Middle name
Last name John Ward

Organization

Texas Chiropractic College

Division name

Research

Zip code


Address

5912 Spencer Highway, Pasadena, TX 77505

TEL

2819985704

Homepage URL


Email

jward@txchiro.edu


Sponsor or person

Institute

Texas Chiropractic College

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2015 Year 05 Month 08 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results

Objective: The purpose of the study was to determine if cervical spinal manipulative therapy (SMT) impacted upper extremity ergometer performance to muscle failure amongst asymptomatic participants.
Methods: Forty-six healthy chiropractic college students were randomized into three study groups using an AB:BA crossover study design with an additional control arm (BB). Each week, of the two-week protocol, participants engaged in a Monark; upper extremity ergometer test at 50 W resistance for females and 100 W for males while maintaining 50 rpm until muscle failure. Group 1(AB) received cervical SMT prior to testing during week one and no SMT prior to testing during week two. Similarly, Group 2(BA) received no SMT week one and SMT week two. Group 3(BB) did not receive SMT either week. Exercise time to exhaustion, exercise heart rate, blood lactate, post 1-min Rating of Perceived Exertion (RPE), and post 5-min RPE were recorded during each session. A paired samples t-test was used to make comparisons between A and B conditions, and to track test acclimation in the BB group.
Results: There was no statistically significant difference between SMT and no-SMT conditions for time to exhaustion (p=0.712), heart rate (p=0.220), blood lactate (p=0.462), post 1-min RPE (0.804) and post 5-min RPE (0.561); however, the week that participants received cervical SMT their heart rate was 8.5 beats higher than the week they did not at test completion.
Conclusions: Preliminarily, this research demonstrates that cervical SMT does not impact upper extremity ergometer performance amongst asymptomatic participants to a statistically significant level.

Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2014 Year 05 Month 01 Day

Date of IRB


Anticipated trial start date

2014 Year 05 Month 02 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2015 Year 02 Month 28 Day


Other

Other related information



Management information

Registered date

2015 Year 05 Month 08 Day

Last modified on

2015 Year 05 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020236


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name