UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040692
Receipt number R000046445
Scientific Title A randomized controlled trial for the intervention effect of early exercise therapy on axial pain after cervical laminoplasty
Date of disclosure of the study information 2020/06/09
Last modified on 2021/11/24 19:19:35

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Basic information

Public title

A study on the effect of exercise therapy on the cervical spine after cervical laminoplasty on the reduction of axial pain

Acronym

A study on the effect of exercise therapy on the cervical spine after cervical laminoplasty on the reduction of axial pain

Scientific Title

A randomized controlled trial for the intervention effect of early exercise therapy on axial pain after cervical laminoplasty

Scientific Title:Acronym

A randomized controlled trial for the intervention effect of early exercise therapy on axial pain after cervical laminoplasty

Region

Japan


Condition

Condition

Cervical Spondylotic Myelopathy
Ossification of the Posterior Longitudinal Ligament

Classification by specialty

Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To determine whether the range of motion training and cervical extension muscle strengthening of the cervical spine from early post-operative cervical laminoplasty can reduce axial pain at 3 months post-operatively.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

axial pain:visual analogue scale(VAS)
Japanese Orthopaedic Association Cervical Myelopathy Evaluation
Questionnaire(JOACMEQ):If you feel pain or stiffness in your neck or shoulders, mark the degree
evaluation period:Pre-op, 2weeks post-op, 3months post-op

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Cervical exercises group
Post-op day 2.
Initiate cervical extensor muscle strengthening and cervical range of motion exercises, education, gait exercises, cervical muscle manual stretching, and postural instruction.
Cervical spine extensor muscle strengthening: 3 sets of 10 isometric muscle strengthening exercises of 5 seconds
Cervical spine range of motion exercises: painless range of motion extension and rotation
Standard intervention frequency: 20 to 40 minutes/day
Post-op day 14.
Discharged after using the pamphlets to teach self-training in cervical extension muscle strengthening and cervical range of motion exercises.
Self-trainingCervical spine extensor muscle strengthening: 3 sets of 10 isometric muscle strengthening for 5 seconds (3 times/day)
Cervical spine range of motion: 5 reps in each direction as long as there is no pain (3 times/day)

Interventions/Control_2

Stretching group
Post-op day 2.
Begin cervical muscular manual stretching, postural instruction, education, and gait practice.
Post-op day 14.
Use the pamphlet to teach good posture

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

40 years-old <=

Age-upper limit

89 years-old >=

Gender

Male and Female

Key inclusion criteria

The criteria for selection are patients between the ages of 40 and 89 who were diagnosed with cervical spondylotic myelopathy or cervical ossification of the posterior longitudinal ligament at Nagoya City Medical Center and who are scheduled for C3-C6 laminoplasty.

Key exclusion criteria

Excludes patients with a history of cervical spine surgery and cerebrovascular accidents, and patients who plan to continue to use the cervical spine collar after surgery.

Target sample size

80


Research contact person

Name of lead principal investigator

1st name Toru
Middle name
Last name Uehara

Organization

Nagoya City West Medical Center

Division name

Physical Medicine and Rehabilitation

Zip code

4628508

Address

1-1-1 Hirate-cho,Kita-ku,Nagoya,Aichi

TEL

0529918121

Email

toru8toru22@gmail.com


Public contact

Name of contact person

1st name Toru
Middle name
Last name Uehara

Organization

Nagoya City West Medical Center

Division name

Physical Medicine and Rehabilitation

Zip code

4628508

Address

1-1-1 Hirate-cho,Kita-ku,Nagoya,Aichi

TEL

0529918121

Homepage URL


Email

toru8toru22@gmail.com


Sponsor or person

Institute

Nagoya City West Medical Center

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Medical Ethics of Hirosaki University Graduate School of Health Sciences

Address

66-1, Hon-cho, Hirosaki-shi, Aomori, 036-8564

Tel

0172395905

Email

jm5905@hirosaki-u.ac.jp


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

2020 Year 06 Month 09 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

124

Results


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

Main results already published

Date of protocol fixation

2019 Year 06 Month 01 Day

Date of IRB

2019 Year 09 Month 24 Day

Anticipated trial start date

2019 Year 12 Month 01 Day

Last follow-up date

2021 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2021 Year 04 Month 30 Day


Other

Other related information



Management information

Registered date

2020 Year 06 Month 09 Day

Last modified on

2021 Year 11 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046445


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name