Multidimensional Cross-sectional Study on Skin Health Based on TCM Constitution - Psychology - Skin Model

November 15, 2017 updated by: Tuya Bao, Beijing University of Chinese Medicine

Beijing University of Chinese Medicine

This survey was designed as a cross-section study investigation, after the selection,the invesgators would adopt the methods of randomly drawing for 100 Beijing female citizens to process: questionnaire survey about the skin health, infrared thermal imaging on facing area, VISIA skin testing and Germany CK company skin testing etc. for integrated evaluation of skin health.

This survey was designed as a cross-section study investigation, after the selection,the invesgators would adopt the methods of randomly drawing for 100 Beijing female citizens to process: questionnaire survey about the skin health, infrared thermal imaging on facing area, VISIA skin testing and Germany CK company skin testing etc. for integrated evaluation of skin health. Analyzing the constitution of volunteers and combining the test related to depression and anxious, psychology health evaluated the healthy states. Base on the data collected processed the statistic analyzing, comprehensive assessment the impact factor of skin health for establishing the Constitution-Psychology-Skin model and though this model to evaluate and forecast the skin health problem.

Study Overview

Status

Unknown

Conditions

Detailed Description

This survey the invesgators designed as a cross-section study investigation, after the selection,the invesgators would adopt the methods of randomly drawing for 100 Beijing female citizens to process: questionnaire survey about the skin health, infrared thermal imaging on facing area, VISIA skin testing and Germany CK company skin testing etc. for integrated evaluation of skin health.

This survey was designed as a cross-section study investigation, after the selection,the invesgators would adopt the methods of randomly drawing for 100 Beijing female citizens to process: questionnaire survey about the skin health, infrared thermal imaging on facing area, VISIA skin testing and Germany CK company skin testing etc. for integrated evaluation of skin health. Analyzing the constitution of volunteers and combining the test related to depression and anxious, psychology health evaluated the healthy states. Base on the data collected processed the statistic analyzing, comprehensive assessment the impact factor of skin health for establishing the Constitution-Psychology-Skin model and though this model to evaluate and forecast the skin health problem.

Standards of included:

  1. Female,
  2. Ages between 18 or above, 55 or below,
  3. Informed consent, voluntary.

Standards of excluded:

  1. Taking part in other surveys before the starting of this survey within 2 months,
  2. Obviously disturbance of consciousness,
  3. Suffering from endocrine systemic disease, mental disease or other severe systemic disease,
  4. Pregnant or lactation period,
  5. Researchers consider that would occur harmful toward volunteers or would affect the aims and the explanation of the results.

The volunteers must require all the above standards would conform to the selection.

Standards of retreat from this survey:

  1. Poor compliance, could not complete all the tests,
  2. Occur any special physiological and pathological changes which not suitable for funder process.

Study Type

Observational

Enrollment (Anticipated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Tuya Bao, PHD
  • Phone Number: 010-6428782 +86 13501090796
  • Email: tuyab@263.net

Study Contact Backup

  • Name: Shixing Feng, Master
  • Phone Number: +86 15201553363
  • Email: fsx@bucm.edu.cn

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

15 years to 55 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

Female,Ages between 18 or above, 55 or below,Informed consent, voluntary.

Description

Inclusion Criteria:

  1. Female,
  2. Ages between 18 or above, 55 or below,
  3. Informed consent, voluntary.

Exclusion Criteria:

Exclusion Criteria:

  1. Taking part in other surveys before the starting of this survey within 2 months,
  2. Obviously disturbance of consciousness,
  3. Suffering from endocrine systemic disease, mental disease or other severe systemic disease,
  4. Pregnant or lactation period,
  5. Researchers consider that would occur harmful toward volunteers or would affect the aims and the explanation of the results.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
PHQ-9
Time Frame: 1 year
PRIME-MD diagnostic instrument for common mental disorders.
1 year
PSQI
Time Frame: 1 year
Despite the prevalence of sleep complaints among psychiatric patients, few questionnaires have been specifically designed to measure sleep quality in clinical populations.
1 year
SCL-90
Time Frame: 1 year
SCL-90 relatively brief self-report psychometric instrument (questionnaire) published by the Clinical Assessment division of the Pearson Assessment & Information group. It is designed to evaluate a broad range of psychological problems and symptoms of psychopathology. It is also used in measuring the progress and outcome of psychiatric and psychological treatments or for research purposes.
1 year
SAS
Time Frame: 1 year
The SAS is a 20-item self-report assessment device built to measure anxiety levels, based on scoring in 4 groups of manifestations: cognitive, autonomic, motor and central nervous system symptoms. Answering the statements a person should indicate how much each statement applies to him or her within a period of one or two weeks prior to taking the test.
1 year
Infrared thermal imaging
Time Frame: 1 year
To measure the condition of the skin.
1 year
VISIA skin testing
Time Frame: 1 year
To measure the condition of the skin.
1 year
Moisture content
Time Frame: 1 year
To measure the condition of the skin.
1 year
Haematochrome test
Time Frame: 1 year
To measure the condition of the skin.
1 year
Elasticity Test of Skin
Time Frame: 1 year
To measure the condition of the skin.
1 year
Skin Sebum Test
Time Frame: 1 year
To measure the condition of the skin.
1 year
Glossiness of Skin
Time Frame: 1 year
To measure the condition of the skin.
1 year
Neuronal Sensitivity
Time Frame: 1 year
To measure the condition of the skin.
1 year
Melanin Test
Time Frame: 1 year
To measure the condition of the skin.
1 year
Chroma of Skin
Time Frame: 1 year
To measure the condition of the skin.
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

November 18, 2017

Primary Completion (Anticipated)

February 15, 2018

Study Completion (Anticipated)

December 30, 2019

Study Registration Dates

First Submitted

October 31, 2017

First Submitted That Met QC Criteria

November 15, 2017

First Posted (Actual)

November 20, 2017

Study Record Updates

Last Update Posted (Actual)

November 20, 2017

Last Update Submitted That Met QC Criteria

November 15, 2017

Last Verified

November 1, 2017

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • BeijingUCMPS

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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