- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05196841
The Effect of Fatima Ana's Hand on Birth Pain and Duration
The Effect of Fatima Ana's Hand (Anastatica Hierochuntica) on Birth Pain and Duration: A Randomized Controlled Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Complementary treatment methods during the birth process are supportive therapies. It is applied to meet the physical and psychological care needs, to help cope with pain during childbirth, to increase the quality of life of pregnant women. Mind-body methods, alternative medical methods, biological-based treatment methods, manipulative and body-based methods, and energy therapy methods are used as complementary treatment methods in labor. The focus applied within the scope of mind-body methods is based on the principle of revealing the mental skill that improve bodily functions. One of the methods applied in this direction is Anastatica Hierochuntica.
Anastatika Hierochuntica is a herbaceous plant that can live 1000-2000 years, with dry leaves resembling a fist-closed hand in which it stores its seeds. Known as "Fatma Ana Eli" or "Meryem Ana Eli". This dry ball-shaped plant in the deserts of Namibia comes alive in the rain and turns to green color by opening the folds. After the rain, the leaves of the plant, which stores some water to pass through a new drought period, close again and take a dry appearance.
The plant Anastatica Hierochuntica is known to have a facilitating effect on labor and is frequently used for this purpose during labor. During childbirth, the Anastatica Hierochuntica plant is dropped into a bowl of water. It is believed that as the plant opens, labor will be easier, and the baby will flow like water.
Despite its frequent use, when the literature is examined, no studies hasve been found on the effect of Anastatica Hierochuntica on birth. For this reason, the study was conducted to evaluate the effect of Anastatica Hierochuntica on labor pain and duration.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Karatay
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Konya, Karatay, Turkey
- KTO Karatay University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having a singleton pregnancy at 38-42 weeks,
- Pregnant women who had spontaneous labor,
- Pregnant women with a healthy fetus,
- Pregnant women without any complications that may cause dystocia during labor,
- Pregnant women who did not receive analgesia and anesthesia during the first phase of labor,
- Planned vaginal delivery, pregnant women who volunteered to participate in the research
Exclusion Criteria:
pregnant women with high-risk pregnancies, Planned caesarean delivery, pregnant women with chronic diseases
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
Anastatica Hierochuntica
|
During the sampling process, the researcher inquired through women who apply for pregnancy follow-up and contacted the mothers who had some inclusion criteria.
Also, the researcher outlined the research plan and objectives.
The participants were assessed based on the eligibility criteria and, if they were eligible and willing to participate in the study.
|
|
No Intervention: Control group
routine care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Severity of labor pain
Time Frame: 12 hours
|
The primary outcomes included the severity of labor pain that was measured by VAS
|
12 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Duration of the active phase of labor
Time Frame: 12 hours
|
The secondary outcomes included the duration of the active phase of labor and the second stage of delivery.
The length of delivery stages was recorded in the partograph chart during labor and childbirth by the researcher.
|
12 hours
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hediye KARAKOC, PhD, Karatay University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KaratayUNI
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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