Multidimensional Cross-sectional Study on Skin Health Based on TCM Constitution - Psychology - Skin Model
Beijing University of Chinese Medicine
1 other identifier
observational
100
0 countries
N/A
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Nov 2017
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 31, 2017
CompletedStudy Start
First participant enrolled
November 18, 2017
CompletedFirst Posted
Study publicly available on registry
November 20, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 15, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2019
CompletedNovember 20, 2017
November 1, 2017
3 months
October 31, 2017
November 15, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (14)
PHQ-9
PRIME-MD diagnostic instrument for common mental disorders.
1 year
PSQI
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
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
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
To measure the condition of the skin.
1 year
VISIA skin testing
To measure the condition of the skin.
1 year
Moisture content
To measure the condition of the skin.
1 year
Haematochrome test
To measure the condition of the skin.
1 year
Elasticity Test of Skin
To measure the condition of the skin.
1 year
Skin Sebum Test
To measure the condition of the skin.
1 year
Glossiness of Skin
To measure the condition of the skin.
1 year
Neuronal Sensitivity
To measure the condition of the skin.
1 year
Melanin Test
To measure the condition of the skin.
1 year
Chroma of Skin
To measure the condition of the skin.
1 year
Eligibility Criteria
Female,Ages between 18 or above, 55 or below,Informed consent, voluntary.
You may qualify if:
- Female,
- Ages between 18 or above, 55 or below,
- Informed consent, voluntary.
You may not qualify if:
- Taking part in other surveys before the starting of this survey within 2 months,
- Obviously disturbance of consciousness,
- Suffering from endocrine systemic disease, mental disease or other severe systemic disease,
- Pregnant or lactation period,
- Researchers consider that would occur harmful toward volunteers or would affect the aims and the explanation of the results.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (1)
Wolf R, Wolf D, Tamir A, Politi Y. Melasma: a mask of stress. Br J Dermatol. 1991 Aug;125(2):192-3. doi: 10.1111/j.1365-2133.1991.tb06075.x. No abstract available.
PMID: 1911305RESULT
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
October 31, 2017
First Posted
November 20, 2017
Study Start
November 18, 2017
Primary Completion
February 15, 2018
Study Completion
December 30, 2019
Last Updated
November 20, 2017
Record last verified: 2017-11