Analgesia, Anxiety, Cesarean Section Complications, Pain, Postoperative
Conditions
Brief summary
The study aim is to examine the relationship between providing information to women prior to elective cesarean delivery and anxiety levels around surgery. the patients will be assigned into two groups - intervention and control. In the intervention group - the day before surgery the women will watch a pre-prepared video showing in detail the course of events around the operation. the level of anxiety, pain level and Intake of Analgesics will be compared between the two groups
Detailed description
Women will be recruited for research at the time of admission preoperatively. According to randomization women will be divided into two groups - intervention and control In the intervention group - the day before surgery the women will watch a pre-prepared video, approximately 10 minutes in length, showing in detail the course of events around the operation - from the woman's perspective - from the time they were admitted to the department, preparation for surgery, entrance to the operating room, anesthesia procedure, surgery Itself, post-operative recovery and recovery course in maternity ward. The movie will be shown to the patient by one of the study investigators. In the control group - women will receive general information about the surgery as part of the routine informed consent process, without watching a pre- prepared film. the level of anxiety, pain level and Intake of Analgesics will be compared between the two groups
Interventions
BEHAVIORALpre-prepared video describing the cesarean surgery
a pre-prepared video, approximately 10 minutes in length, showing in detail the course of events around the operation - from the woman's perspective - from the time they were admitted to the department, preparation for surgery, entrance to the operating r
BEHAVIORALgeneral information
In the control group - women will receive general information about the surgery as part of informed consent, without watching a pre-prepared film.
Sponsors
HaEmek Medical Center, Israel
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Caregiver)
Intervention model description
Women will be recruited for research at the time of admission preoperatively According to randomization women will be divided into two groups - intervention and control
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* First cesarean surgery
Exclusion criteria
* Women who have had surgery beyond age 2 years * Women with anxiety disorders * Women with comorbidity that might alter cortisol and catecholamine excretion, * Women with comorbidity associated with severe pain that might distort pain ratings * Women with psychiatric comorbidity that might reduce the ability to understand the videotape and questionnaires * Women who consume any medication that might affect urinary excretion of cortisol * Women undergoing cesarean surgery due to obstetric complication (gestational hypertension, pre-eclampsia, gestational diabetes mellitus)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The difference in anxiety level between the two groups at one hour before surgery. | 3 points: before watching the movie (t1), one hour before surgery (t2), 8 hours after the surgery (t3). | To assess a patient's anxiety response to a given situation, the investigators will use State Trait Anxiety Scale (STAI) questionnaire. The questionnaire consists of two sets of 20 different questions that can be answered from 1 to 4. The first (state subscale) assesses a current anxiety condition, while the second (trait subscale) assesses personality characteristics. This questionnaire was found to be valid for use in a study of a pregnant women population. High scores indicate high levels of anxiety Although the outcome is the The difference in anxiety level between the two groups at one hour before surgery, the investigators will assess the baseline anxiety level and 8 hours after the surgery, for inter-group comparison. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Maternal complications | during the time of hospitalization after delivery, up to 1 month | any obstetrical complication |
| Change from baseline pain level at 8 hours after surgery | 3 points: before watching the movie (t1), one hour before the surgery (t2), 8 hours after the surgery (t3). | To assess a patient's pain level, the investigators will use visual analog scale (VAS)- scale for patient self-reporting of pain. 0 represents no pain, 1-3 represents mild pain, 4-6 represents moderate pain, 7-10 represents severe pain). a lower pain level 8 hours after surgery is a better outcome Although the outcome is the change from baseline level at 8 hours after the surgery, the investigators will assess the pain level before the surgery for inter-group comparison. |
| Change from baseline biochemical anxiety level at 6 hours interval following the surgery | 2 points: the morning before surgery (c1) and 6 hours following the surgery (c2) | Cortisol blood levels taken 6 hours following the surgery. Although the outcome is the change from baseline level at 6 hours following the surgery, the investigators will assess the cortisol level 6 hours after the surgery for inter-group comparison. |
Countries
Israel
Contacts
Primary Contacteyal rom, MD
Outcome results
None listed