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Randomized Controlled Trial of a Psychoeducational Web Application for Social Anxiety in Social Situations.

A Randomized Controlled trial of a Psychoeducational Web Application for Social Anxiety in Social Situations. - RCT of a Psychoeducational Web Application for Social Anxiety in Social Situations.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060669
Enrollment
60
Registered
2026-02-18
Start date
2026-02-20
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Social Anxiety.

Interventions

web-based app education based on cognitive behavioral theory No treatment(During the exam period, access the web daily and enter information such as the day&#39
s weather.)

Sponsors

Department of Cognitive Behavioral Physiology ,Chiba University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Individuals aged 18 years or older but under 65 years at the time of consent. 2) Individuals who have never previously visited a psychiatrist or psychosomatic medicine specialist and are not currently receiving treatment from one. 3) Individuals working 20 hours or more per week. 4) Individuals with a total score of 19 points or higher on the Social Phobia Inventory (SPIN). 5) Individuals who do not meet the diagnostic criteria for social anxiety disorder (based on the American Psychiatric Association's DSM-5-TR). 6) Individuals who, prior to participating in this trial, received explanations via web-based documents and video, and provided informed consent online of their own free will after achieving sufficient understanding. 7) Individuals with internet access and a computer environment capable of using web-based applications.

Exclusion criteria

Exclusion criteria: 1) Individuals for whom contact with researchers is difficult. 2) Other individuals deemed unsuitable by the principal investigator or research collaborators for the safe conduct of this study. 3) Individuals at risk of suicide (those scoring 2 to 3 points on item 9 of the PHQ-9 depression scale, which assesses suicidal ideation).

Design outcomes

Primary

MeasureTime frame
Change (difference) in SPIN total score from week 0 (baseline) to week 6

Secondary

MeasureTime frame
Secondary outcomes are as follows: - Change (difference) from week 0 (baseline) in the SPIN total score at week 12 (follow-up) - Change (difference) from pre-intervention baseline to post-intervention scores for the depression scale PHQ-9, social anxiety scale LSAS, quality of life scale EQ-5D-5L, and anxiety scale GAD-7 at weeks 6 and 12

Countries

Japan

Contacts

Public ContactShuhei Aoki

Chiba University Graduate School of Medicine Department of Cognitive Behavioral Physiology

25fd1101@student.gs.chiba-u.jp043-226-2027

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026