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The efficacy of online EMDR for PTSD patients: a randomized controlled single-blind trial

The efficacy of online EMDR for PTSD patients: a randomized controlled single-blind trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059328
Enrollment
Unknown
Registered
2022-04-28
Start date
2022-01-21
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

Post-traumatic stress disorder

Interventions

Online EMDR treatment group:Online EMDR

Sponsors

Beijing Anding Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of DSM-5 for PTSD; 2. Applicants must be between 18 and 65 years of age, regardless of gender, and have received education >9 years; 3. The subjects or their family members signed the informed consent and complied with the study protocol; 4. If the patients with other mental diseases, the condition is stable for more than 1 month; 5. Familiar with mobile phones, tablet computers and other electronic products

Exclusion criteria

Exclusion criteria: 1. Have participated in or are currently participating in EMDR or trauma-focused psychotherapy; 2. Patients with neurological diseases or eye diseases; 3. Currently suicidal, extremely agitated or incompatible with the author.

Design outcomes

Primary

MeasureTime frame
Clinician-Administered PTSD Scale;

Secondary

MeasureTime frame
Impact of Event Scale-Revised;Self-rating Depression Scale;Self-rating Anxiety Scale;Symptom check list 90;Head MRI;

Countries

China

Contacts

Public ContactXianbin Li

Beijing Anding Hospital, Capital Medical University

xianbinli@ccmu.edu.cn+86 010-58303117

Outcome results

None listed

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