Clinical trial program "nurse companionship" on health outcomes of mothers undergoing cesarean section

The effect of "nurse companionship" program on health outcomes of mothers undergoing cesarean section

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016081727561N3

Enrollment

128

Registered

2016-12-09

Start date

2016-10-22

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

Health outcomes of mothers candidate for cesarean section. Counselling, unspecified

Interventions

Intervention 1: Control group: This routine care includes: accepted the mother in the unit, preparing file, check out routine tests of cesarean section, wear of surgery gun, notice and transfer to th

Behavior

Control group: This routine care includes: accepted the mother in the unit, preparing file, check out routine tests of cesarean section, wear of surgery gun, notice and transfer to the operating roo

Intervention group: Mother candidate for cesarean in addition to receive routine care, will get nurse support and companionship 1 hour before the surgery starts until the 1 hour after the surgery. T

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Candidate for cesarean, Mothers with Non-emergency cases? No nulliparous mothers? Mothers consciousness enough to cooperate? Effective communication between mothers and nurses? No maternal history of allergy to spinal anesthesia? No high risk situation for the baby? Single and term pregnancy. Exclusion Criteria: Unsuccessful spinal anesthesia, Receive general anesthesia? Need another surgery (Hysterectomy)? History of taking Anti-anxiety drugs? Suffering from any mental problems? History of Kidney disease, Cardiovascular disease, Hearing problem and etc.? History of Gestational diabetes, Preeclampsia, Polyhydramnios and etc? History of HIV And Hepatitis? Any thing out of the surgerys routines occur in surgery? Want to exit the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Anxiety. Timepoint: 1 hour before and 1 hour after the surgery. Method of measurement: Spielberger anxiety questionnaire.;Pain. Timepoint: 1 Hour before surgery, when the mother is placed on surgery bed and 1 hour after surgery. Method of measurement: Visual analogue scale (VAS).;Vital sign. Timepoint: 1 Hour before surgery, when the mother is placed on surgery bed and 1 hour after surgery. Method of measurement: Digital blood pressure monitor ALPK.	—

Measure

Time frame

Anxiety. Timepoint: 1 hour before and 1 hour after the surgery. Method of measurement: Spielberger anxiety questionnaire.;Pain. Timepoint: 1 Hour before surgery, when the mother is placed on surgery bed and 1 hour after surgery. Method of measurement: Visual analogue scale (VAS).;Vital sign. Timepoint: 1 Hour before surgery, when the mother is placed on surgery bed and 1 hour after surgery. Method of measurement: Digital blood pressure monitor ALPK.

—

Secondary

Measure	Time frame
Satisfaction. Timepoint: 1 Hour after surgery. Method of measurement: Tabbi patient’s satisfaction questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElnaz Asghari

Tabriz University of Medical Sciences

asghari.elnaz@gmail.com+98 41 3479 6969

Outcome results

None listed

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