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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT00917332
Other study ID # 0256-09-HMO
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 8, 2009
Last updated June 9, 2009
Start date August 2009
Est. completion date November 2009

Study information

Verified date June 2009
Source Hadassah Medical Organization
Contact efrat esterkin, MA
Email efratkin@gmail.com
Is FDA regulated No
Health authority Israel: Ethics Commission
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether relaxation and guided imagery techniques are effective in reducing childbirth pain.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 110
Est. completion date November 2009
Est. primary completion date October 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- women who carry their first child

- women that carry only one embryo

- women who speaks hebrew

Exclusion Criteria:

- women who experienced complications in pregnancy.

- women who planning on having an elective Caesarean section.

- women who suffer from background systematic condition (such as high-BP, diabetes).

- women who have psychiatric background.

- women who take chronic medication that might effect childbirth, woman or baby's health.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Behavioral:
relaxation (breathing and muscles) and guided imagery ("safe place")
intervention group: daily practice of relaxation and guided imagery CD, for a rew weeks, until childbirth.

Locations

Country Name City State
Israel Hadassah Ein-Kerem Haspitol Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary rating of pain experienced during childbirth on pain VAS one time - during hospitalization after childbirth No
Secondary rate and the starting time of receiving regional anesthesia (epidural) at childbirth No