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Evaluation of the Impact of Online Mindfulness Intervention on the Mental Health of Nursing Students using Portable EEG Collection Device

Evaluation of the Impact of Online Mindfulness Intervention on the Mental Health of Nursing Students using Portable EEG Collection Device

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080314
Enrollment
Unknown
Registered
2024-01-25
Start date
2024-01-31
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

mental disorders

Interventions

Mindfulness Intervention with EEG Feedback Group:Participants will undergo a 6-week mindfulness intervention program, consisting of two sessions per week. Throughout the mindfulness meditation, partic
Mindfulness Intervention Group:Participants will undergo a 6-week mindfulness intervention program, consisting of two sessions per week.
Control Group:Participants will receive health education materials unrelated to the intervention content over the same 6-week period.

Sponsors

School of Population Medicine and Public Health, Chinese Academy of Medical Sciences & Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 26 Years

Inclusion criteria

Inclusion criteria: I. Undergraduate and graduate students in the nursing program at Peking Union Medical College who are 18 years old or above; II. Ability to independently cooperate to complete various questionnaire assessments and EEG collection; III. Possession of mobile phone that can be connected to the internet at any time and the Bluetooth function of the phone is normal; IV. Right handedness; V. Willingness to participate throughout the entire process, providing informed consent, and signing the electronic version of the informed consent form as required by the ethics committee.

Exclusion criteria

Exclusion criteria: I. Individuals who are on leave of absence, suspended, or have withdrawn from the study during the research period. II.individuals who have obvious scars on the forehead skin or other unsuitable conditions for EEG collection; III. Individuals suffering from severe internal medical conditions such as heart, brain, lung, kidney, liver diseases, or other unsuitable conditions for research; IV. Individuals unable to cooperate with the investigation or intervention; V. Participants in other health promotion or clinical intervention studies.

Design outcomes

Primary

MeasureTime frame
Electroencephalogram;anxiety symptoms;symptoms of depression; Resilience;Mindfulness;Perceived Social Support;

Secondary

MeasureTime frame
sleep quality;Fatigue;Acceptance of intervention materials;

Countries

China

Contacts

Public ContactXiaoyou Su

School of Population Medicine and Public Health, Chinese Academy of Medical Sciences & Peking Union Medical College

suxiaoyou@hotmail.com+86 10 6510 5830

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026