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Acupoint Thermal Radiation Characteristics in Adolescents with MDD

Acupoint Thermal Radiation Characteristics in Adolescents with Major Depressive Disorder and Establishment of Diagnostic Model

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06750640
Enrollment
100
Registered
2024-12-27
Start date
2022-03-05
Completion date
2024-11-30
Last updated
2024-12-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depression

Keywords

Major Depression Disorder, acupoint temperature, adolescent

Brief summary

Modern studies have confirmed that skin temperature changes at acupoints when the body is under pathological conditions. This suggests that changes in the thermal radiation characteristics of acupoints can objectively respond to the symptoms of a disease. In this study, the investigators first evaluated reproducibility of acupoint temperature measurement by IRT. Secondly, the investigators explored the thermal radiation characteristics of MDD-related acupoints, built the diagnostic model for adolescent depression severity and the diagnostic model for MDD in adolescents based on acupoint temperature. Our research findings will provide new ideas, methods and visualisations for early screening, auxiliary diagnosis and condition assessment of MDD in adolescents.

Detailed description

A total of 100 subjects were included, 60 adolescent with MDD (MDD group) and 40 healthy controls (HC group). All subjects accepted IRT detection.The random selection of 30 adolescent with MDD allowed the collection of the bilateral same name acupoint temperatures. Intra- and inter-observer reproducibility for the patients were examined in some randomly selected patients by 2 investigators and 2 investigators both made 2 independent measurements in a week. 30 MDD subjects were detected the bilateral same name acupoint temperatures.

Interventions

DIAGNOSTIC_TESTInfrared thermography

A thermograph (NEC InfRec R450, Avio Infrared Technologies Co., Ltd., Tokyo) was used to record thermal images. The infrared camera was fixed on a tripod 1 m away from the subject to ensure that no shaking movements or vibrations occurred during the recording of thermal images. MDD related acupoints on the inner and outer sides of the limbs were detected. Appropriate body position was selected according to the different parts to be detected. Using the automatic interval saving shooting mode, one thermal picture was taken at 10-s intervals, 3 pictures were taken for each subject.

Sponsors

Zhejiang Provincial Tongde Hospital
CollaboratorOTHER
First People's Hospital of Hangzhou
CollaboratorOTHER
Xiaomei Shao
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion criteria for the healthy control participants: * 12years≤ age\<18 years; * SDS score \<53; * Adolescents with normal cognitive function can cooperate with the study; * Adolescents and guardians agree to the study plan and sign the informed consent form. Inclusion criteria for the major depression disorder participants: * 12years≤ age\<18 years; * Self-rating Depression Scale (SDS) score ≥ 53; * Language, cognition and communication ability are normal; * Patients and guardians agree to the study plan and sign the informed consent form.

Design outcomes

Primary

MeasureTime frameDescription
Acupoint emperatureBaselineTemperature of acupoints was measured by infrared thermography (IRT). IRT was not be performed on female subjects during their menstrual and ovulatory periods.

Secondary

MeasureTime frameDescription
The Self-Rating Depression Scale (SDS) ScoresBaselineThe standard score is the total of all scores multiplied by 1.25 to the nearest whole number on this scale, which has 20 questions. A standard score below 53 is normal; 53-62 is mild depression; 63-72 is moderate depression; 72 or more is severe depression.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026