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Efficacy of Self-hypnosis combined with Citalopram on the Stait- Trait Anxiety in patients with Generalized Anxiety Disorder and Quality of Life

Efficacy of Self-hypnosis combined with Citalopram on the Anxiety in patients with Generalized Anxiety Disorder and Quality of Life

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015091023966N1
Enrollment
20
Registered
2015-12-21
Start date
2013-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Generalized Anxiety Disorder. Anxiety that is generalized and persistent but not restricted to, or even strongly predominating in, any particular environmental circumstances (i.e. it is

Interventions

Intervention 1: Self hypnosis Training: for experimental groups and for 6 weeks. Intervention 2: Citalopram: In this research in the form of tablets of 20 mg was prescribed once a day for 6 weeks for
Behavior
Treatment - Drugs
Self hypnosis Training: for experimental groups and for 6 weeks.
Citalopram: In this research in the form of tablets of 20 mg was prescribed once a day for 6 weeks for both of experimental and control groups.
Without self-hypnosis training sessions: for the Control group as a shame of interview for 6 weeks

Sponsors

Vice chancellor for research, Semnan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Diagnosis of Generalized Anxiety Disorder (GAD) by psychiatrist; Without comorbid disorders; To have not severe physical illness Exclusion criteria: Under treatment or other educational program ; The absence of more than two sessions

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Generalized Anxiety Disorder. Timepoint: Baseline-After intervention-Two months after intervention. Method of measurement: Spielberger's State-Trait Anxiety Inventory.;Quality of Life. Timepoint: Baseline- After the intervention-Two months after the intervention. Method of measurement: The World Health Organization Quality of Life Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Moghanizadeh

Mashhad University of Medical Sciences

moghaniz2@mums.ac.ir+98 513854464333

Outcome results

None listed

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