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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05836181
Other study ID # TSGHNDMC
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2014
Est. completion date December 28, 2016

Study information

Verified date April 2023
Source National Defense Medical Center, Taiwan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Eye Movement Desensitization and Reprocessing intervention may improve anxiety, depression, systolic blood pressure and heart rate variability in patients with hypertension.


Recruitment information / eligibility

Status Completed
Enrollment 110
Est. completion date December 28, 2016
Est. primary completion date December 10, 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria: 1. age of 20-80 years, 2. diagnosed with primary hypertension as in SBP =130 mmHg or DBP =80 mmHg, 3. and able to read and understand Chinese or Taiwanese and willing to participate in this study, Exclusion Criteria: 1. . Secondary hypertension 2. . Hypertension Crisis.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Eye Movement Desensitization and Reprocessing
Effects of Eye Movement Desensitization and Reprocessing on Anxiety, Depression, Quality of Life, Blood Pressure and Heart Rate Variability in Patients with Hypertension.

Locations

Country Name City State
Taiwan Chen, miao-yi Taipei Neihu

Sponsors (1)

Lead Sponsor Collaborator
Miao-Yi Chen

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anxiety HADS-A score Six month
Primary depression symptoms CESD Scale Six month
Secondary Blood pressure Blood pressure Six month
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