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The compare of effects of nursing consultation in three groups of face to face, distance and control on symptoms of post traumatic stress disorder

Clinical trial comparing the effects of nursing consultation in three groups of face to face, distance and control on symptoms of post traumatic stress disorder

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201410268978N2
Enrollment
90
Registered
2017-01-05
Start date
2015-05-22
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

post traumatic stress disorder. post traumatic stress disorder

Interventions

Treatment - Other
Treatment - Drugs
Intervention 1: nursing face to face consultation is conducted in six sessions, once every two weeks.?
Intervention 1: Intervention 1: nursing face to face consultation is conducted in six sessions, once every two weeks.?. Intervention 2: Intervention 2: nursing distance consultation is conducted in si
Intervention 2: nursing distance consultation is conducted in six sessions once every two weeks via ?internet.?
Control group: this group is a waiting list and for ?three months do not receive any counseling.?

Sponsors

Vice chancellor for research, Tehran University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 18 to 70 years; settled in Guilan; pass a month of physical injury, ?subsequent motor vehicle accidents; having at least two positive symptoms on each clusters ?symptoms; anesthesia less than 15 minutes after the accident; internet access and have experience ?of using personal email; lack of current psychiatric severe disease (psychosis and mania); organic ?brain disease and serious internal disease; lack of serious physical harm Exclusion criteria: under of the psychiatric treatment; having thought and intent of suicide; having ?thought and intent of homicide

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post traumatic stress disorder symptoms. Timepoint: immediately before and three months after intervention. Method of measurement: Post traumatic stress disorder symptom scale.

Secondary

MeasureTime frame
Depression. Timepoint: immediately before and three months after intervention. Method of measurement: Beck depression inventory 2.;Quality of life. Timepoint: immediately before and three months after intervention. Method of measurement: questionnaire quality of life.;Pain. Timepoint: immediately before and three months after intervention. Method of measurement: the numeric rating scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaema Khodadady

Tehran University of Medical Science

n_khodadady@yahoo.com+98 13 3350 3201

Outcome results

None listed

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