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Research on Personalised Anxiety Intervention Programmes Based on Restorative Environments

Research on Personalised Anxiety Intervention Programmes Based on Restorative Environments

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111935
Enrollment
Unknown
Registered
2025-11-07
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Anxiety

Interventions

Visual Neural Feedback Group:Intervention using neurofeedback based on brain asymmetry to modulate parameters of restorative environmental imagery
Visual Group:Employing imagery of natural elements to guide mindfulness practice within restorative environments for intervention
Tactile Group:Interventions combining wearable device vibration-guided mindfulness with restorative environments for intervention
Auditory Group:Employing natural sounds to guide mindfulness in conjunction with restorative environments for intervention
Olfactory Group:Employing natural scents to guide mindfulness in conjunction with restorative environments for therapeutic intervention

Sponsors

School of Design, Hunan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Students or workers: spending over 8 hours daily in indoor studios. (2) Anxiety-prone individuals: scoring over 50 on the Self-Rating Anxiety Scale (SAS). (3) Aged between 18 and 60 years. (4) Possessing sound cognitive function with no impairment in activities of daily living. (5) No hearing loss, with normal vision or corrected to normal.

Exclusion criteria

Exclusion criteria: (1) The patient suffers from severe cardiovascular, hepatic, renal, or haematopoietic system disorders. 2) The patient's anxiety stems from psychiatric disorders (such as depression or Parkinson's disease). 3) The patient has a history of epilepsy or currently experiences uncontrolled epileptic seizures. (4) The patient has taken antidepressants or antipsychotic medications within the two weeks preceding the trial. (5) The patient suffers from severe motion sickness or has an allergy to contact with wearable devices.

Design outcomes

Primary

MeasureTime frame
Electroencephalogram (EEG);State-Trait Anxiety Inventory(STAI);Perceived Recoverability Scale(PRS);

Secondary

MeasureTime frame
Heart Rate (HR);Gender;(FAA);

Countries

China

Contacts

Public ContactHanling Zhang

School of Design, Hunan University

jt_hlzhang@hnu.edu.cn+86 731 8882 2405

Outcome results

None listed

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