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The comparison of Teach Back educational method and accompanying person on anxiety and vital signs changes in woman candidate for cesarean section

The comparison of Teach Back educational method and accompanying person on anxiety and vital signs changes in woman candidate for cesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014041417270N1
Enrollment
90
Registered
2014-10-29
Start date
2014-07-05
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

surgical anxiety. Neurotic, stress-related and somatoform disorders

Interventions

Intervention 1: second intervention group is the Accompanying Person group.In this group, routine training provided by the ward nurse and their partner were allowed to present next to them from the ni
Prevention
second intervention group is the Accompanying Person group.In this group, routine training provided by the ward nurse and their partner were allowed to present next to them from the night before the s
First intervention group is the Teach Back group. In this group individuals were educated by using Teach Back method in this way that after determining training needs, educational program that is appr
Control group is the third group whom no intervention applyed to them except routine educations.

Sponsors

Vice Chancellor for research of Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 30 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 20 to 30 years old, not treated with anxiolytic or sedative drugs during hospitalization, have consent to participate in the study have moderate(41-60) or severe(61-80) anxiety according to the STAI and candidate for the first cesarean section. Exclusion criteria: psychological disorders, hearing loss, and unwillingness to continue participation in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety before surgery. Timepoint: the night beore surgery and the day of the surgery. Method of measurement: Spiel Berger State-Trait Anxiety inventory.

Secondary

MeasureTime frame
Systole Blood Pressure. Timepoint: Night Before The Surgery (Before Intervention)and Day of The Surgery(After Intervention). Method of measurement: mmHg- Electronic Manometer(Beurer made in Germany).;Diastole Blood Pressure. Timepoint: Night Before The Surgery (Before Intervention)and Day of The Surgery(After Intervention). Method of measurement: mmHg- Electronic Manometer(Beurer made in Germany).;Respiratory Rate. Timepoint: Night Before The Surgery (Before Intervention)and Day of The Surgery(After Intervention). Method of measurement: Number in minute by using analog clock and numeration.;Pulse Rate. Timepoint: Night Before The Surgery (Before Intervention)and Day of The Surgery(After Intervention). Method of measurement: Number in minute by using analog clock and numeration.;Temperature. Timepoint: Night Before The Surgery (Before Intervention)and Day of The Surgery(After Intervention). Method of measurement: Mercury thermometer made in iran.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasim Hatefi Moadab

Ahvaz Jundishapur University of Medical Sciences

hatefi.n@ajums.ac.ir+98 83 3424 2764

Outcome results

None listed

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