UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000046171
Receipt number R000052475
Scientific Title The comparison of cd-risc and NEO-FFI psychological and biological factors in woman with and without upper cross syndrome(ucs)
Date of disclosure of the study information 2021/12/20
Last modified on 2021/11/25 00:34:50

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Basic information

Public title

The comparison of psychological factors in woman with and without upper cross syndrome

Acronym

TCOPFIWWAWUCS

Scientific Title

The comparison of cd-risc and NEO-FFI psychological and biological factors in woman with and without upper cross syndrome(ucs)

Scientific Title:Acronym

TCOCANPABFIWWAWUCS

Region

Asia(except Japan)


Condition

Condition

control condition
This study was performed in women with and without upper cross syndrome with different backgrounds(university student, employeess of health sectors)

Classification by specialty

Psychiatry Rehabilitation medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Comparison of biological factors(FMS,Q Angle and BMI) in woman with and without upper cross syndrome

Basic objectives2

Others

Basic objectives -Others

Comparison of psychological factors(CD-RISC and NEO-FFI) in woman with and without upper cross syndrome

Trial characteristics_1

Confirmatory

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

In this study it was confirmed that FMS,Q angle and BMI had no meaningful impact in our women study group with and without upper cross syndrome

Key secondary outcomes

It was also confirmed that psychological factors evaluated with cd-risc and neo-FFI had no meaningful impact in women with and without cs


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification

YES

Dynamic allocation

YES

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

No need to know


Intervention

No. of arms

1

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Behavior,custom

Interventions/Control_1

uncontrol

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

30 years-old >=

Gender

Female

Key inclusion criteria

female between 20-30 years old in tehran

Key exclusion criteria

male- people with disability and cardiac health issues

Target sample size

70


Research contact person

Name of lead principal investigator

1st name Farnaz
Middle name
Last name Tajmehrabinamin

Organization

Islamic Azad University Science and Research Branch

Division name

Hmanities

Zip code

00000

Address

Iran, Tehran, Sattari highway, Daneshgah blvd

TEL

00989359665520

Email

f.tajmehrabi@gmail.com


Public contact

Name of contact person

1st name Farnaz
Middle name
Last name tajmehrabinamin

Organization

Islamic Azad University Science and Research Branch

Division name

hmanities faculty

Zip code

00000

Address

Tehran, sattari highway, daneshgah Blvd.

TEL

00982144865154

Homepage URL


Email

humanities-fa@srbiau.ac.ir


Sponsor or person

Institute

Islamic Azad University Science and Research Branch

Institute

Department

Personal name



Funding Source

Organization

self funding

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

iran


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

ministry of health and medical education national research ethics committee

Address

Tehran, quds west, simaye Iran street ministry of health and medical education block A 13th floor

Tel

00982181455618

Email

ethics@behdasht.gov.com


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

polymer and petrochemical institute(Tehran)sport center clinic(Tehran)
Iranian blood transfusion organization , Tehran blood transfusion department


Other administrative information

Date of disclosure of the study information

2021 Year 12 Month 20 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

70

Results

there are no significant difference between woman with and without upper cross syndrome in psychological and biological factors

Results date posted

2021 Year 11 Month 25 Day

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

2019 Year 11 Month 18 Day

Date of IRB

2021 Year 02 Month 28 Day

Anticipated trial start date

2020 Year 09 Month 12 Day

Last follow-up date

2020 Year 12 Month 17 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2021 Year 11 Month 25 Day

Last modified on

2021 Year 11 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000052475


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name