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Acute Effects of Cold Exposure on Cognitive Function

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Fudan University

Status

Active, not recruiting

Conditions

Cognitive Function

Treatments

Other: Moderate temperature (22℃) group
Other: Low temperature (15℃) group

Study type

Interventional

Funder types

Other

Identifiers

NCT06654167
IRB#2024-10-1168

Details and patient eligibility

About

This is a randomized controlled human exposure crossover study. Investigators aims to assess the acute effects of low-temperature exposure on cognitive function and the underlying mechanisms.

Full description

The investigators will conduct a randomized controlled human exposure crossover study among about 40 healthy young adults in Shanghai, China. Each subject will be exposed twice: once to the low temperature (15℃) and once to the moderate temperature (22℃) in a chamber for about 2 hours. During the exposure session, each subject will be requested to rest. Health examinations will be conducted immediately prior to exposure, during the period of exposure, and after exposure. Health examinations include cognitive function tests and magnetic resonance imaging. Investigators plan to collect blood and urine samples.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Living in Shanghai during the study period;
  • Body mass index > 18.5 and ≤ 28;
  • right-handed;
  • receiving or having received higher education;
  • with the ability to read and understand Chinese smoothly.

Exclusion criteria

  • Smoking and alcohol abuse;
  • Current drug and dietary supplements intake;
  • Subjects with allergic diseases, such as allergic rhinitis, allergic asthma, and atopy;
  • Subjects with cardiovascular diseases, such as congenital heart disease, pulmonary heart disease, and hypertension;
  • Subjects with respiratory diseases, such as asthma, chronic bronchitis, and chronic obstructive pulmonary disease;
  • Subjects with chronic diseases, such as diabetes, chronic hepatitis, and kidney disease;
  • Subjects who have a history of major surgery due to the cardiovascular, cerebrovascular, respiratory, or neurological diseases;
  • Subjects with neurologic disorders, such as stroke, traumatic brain injury, epilepsy, and schizophrenia;
  • Abnormal spirometry (FEV1 and FVC ≤ 75% of predicted and FEV1/FVC ≤ 0.65);
  • Subjects with color vision disabilities.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

40 participants in 2 patient groups

Low temperature (15℃) group
Experimental group
Description:
Subjects in the exposure group will be exposed to low temperature (15℃) for about 2 hours in a chamber.
Treatment:
Other: Low temperature (15℃) group
Moderate temperature (22℃) group
Experimental group
Description:
Subjects in the exposure group will be exposed to moderate temperature (22℃) for about 2 hours in a chamber.
Treatment:
Other: Moderate temperature (22℃) group

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Renjie Chen, PhD; Haidong Kan, PhD

Data sourced from clinicaltrials.gov

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