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Wearable device data collection and follow-up in the population with insomnia and mood disnormality

Wearable device data collection and follow-up in the population with insomnia and mood disnormality

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108481
Enrollment
Unknown
Registered
2025-09-01
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Insomnia and mood disnormality

Interventions

Intervention group:There are weekly videos or lessons or articles (4-5 per week) to provide psychological education about insomnia and strategies to help solve their sleep and mood problems.
Control group :None

Sponsors

Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Control Group Inclusion Criteria: 1. Age>=18 years old; 2. Have Chinese reading, writing, and communication skills, and be able to use the Huawei Health app independently. 3. Provide written informed consent and voluntarily participate in this project; Intervention group inclusion criteria: 1. Age>=18 years old; 2. Have Chinese reading, writing, and communication skills, and be able to use the Huawei Health app independently. 3. Provide written informed consent and voluntarily participate in this project;

Exclusion criteria

Exclusion criteria: Control group exclusion criteria: 1. Refuse to use social media and sign informed consent; 2. Life expectancy within 1 year (history of malignant tumors); 3. History of sleep disorders except for primary insomnia, including sleep apnea syndrome, restless legs syndrome, narcolepsy, REM sleep behavior disorder, somnambulism, etc.; Intervention group exclusion criteria: 1. Refuse to use social media and sign informed consent; 2. Life expectancy within 1 year (history of malignant tumors); 3. Those who suffer from serious chronic diseases, are at risk of sudden adverse events (such as arrhythmia, cardiac arrest, syncope, epilepsy, shock, cardiovascular and cerebrovascular accidents, fractures, etc.), or are unable to live independently, or are unable to perform sports training or have obvious risk of injury; 4. History of sleep disorders excluding primary insomnia, including sleep apnea syndrome, restless legs syndrome, narcolepsy, REM sleep behavior disorder, somnambulism, etc.; 5. Self-Rating Depression Scale (SDS) score greater than 72 points (major depression); 6. Self-rating anxiety scale (SAS) score greater than 69 points (severe anxiety);

Design outcomes

Primary

MeasureTime frame
Pittsburgh Sleep Quality Index, PSQI;Stress Perception Scale score;Self-Rating Depression Scale score;Anxiety self-rating scale score;

Secondary

MeasureTime frame
Physicial exercise amount;Heart rate variability ;Weekly questionaire;

Countries

China

Contacts

Public ContactDing Fengfei

Fudan University, School of Basic Medical Sciences

Fengfei_ding@fudan.edu.cn+86 134 7625 5813

Outcome results

None listed

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