The primary objective is to examine whether the pain threshold during pregnancy is associated with the intensity of the pain and whether there is difference between before and during pregnancy. In addition, we examine associations between (pro)…
ID
Source
Brief title
Condition
- Other condition
- Pregnancy, labour, delivery and postpartum conditions
Synonym
Health condition
zwangerschapswens
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The proposed study will provide data of the pain threshold before and during
pregnancy and the intensity of pain during labour.
Secondary outcome
Secondary parameters are (pro) inflammatory status, constitution of the woman,
her relationship and the character of the partner.
Background summary
Pain experienced by women during childbirth is the most intense acute pain.
During labour 60 - 80% of the women experiences severe to unbearable pain. Some
factors have their positive (self-efficacy, pregnancy course) or negative
influence (anxiety, stress and low back pain during menstruation) to the pain
intensity. Knowledge about other factors before or during pregnancy that can
predict the severity of labour pain are hardly available due to the high global
use (> 60%) of epidural analgesia during labour. In the Netherlands, the use of
epidural analgesia is relatively low (± 10%). This study can obtained insights
about the pain threshold, pro inflammatory status, constitution of the woman,
her relationship and the character of her partner and their impact on the
intensity of pain during labour.
Study objective
The primary objective is to examine whether the pain threshold during pregnancy
is associated with the intensity of the pain and whether there is difference
between before and during pregnancy. In addition, we examine associations
between (pro) inflammatory status, the constitution of the woman, the
relationship with her partner and the character of her partner.
Study design
The proposed study is an observational prospective cohort study.
Study burden and risks
The burden of the participants consists of measuring the pain threshold (2 x
half hours) or the venapuntion (2 x 5 min, 30 ml total) during a home visit and
filling out the questionnaires (total 2 hours). Also there is a burden to
obtain the VAS during labour.
The risk with participation of the study is small and is related to algometry
(haematoma or pain on the pressure point), the venapunction (risk of fainting
or haematoma) or filling out the questionnaires (stress) during a home visit.
Lundlaan 6
3584 EA Utrecht
Nederland
Lundlaan 6
3584 EA Utrecht
Nederland
Listed location countries
Age
Inclusion criteria
pregnancy wish or primigravidity
age from 18 years
control of dutch language
informed consent
Exclusion criteria
Women with rheumatic disorders which are connected with pain e.g. rheumatoid arthritis.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL23135.041.08 |