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The Effect of Consumption of Date Fruit and Nipple Stimulation in Late Pregnancy

The Effect of Consumption of Date Fruit and Nipple Stimulation in Late Pregnancy on The First Stage of Labor

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06280911
Enrollment
198
Registered
2024-02-28
Start date
2013-10-10
Completion date
2017-12-30
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Augmentation, Induction, Labor, Stimulation, Self

Keywords

Augmentation, Date fruit, Induction, Labor, Nipple Stimulation

Brief summary

The study was conducted to determine the effect of consumption of date fruit and nipple stimulation on labor. The samples were applied to pregnant women satisfying the research criteria in a state hospital in Istanbul between October 2013 and June 2014.

Detailed description

The study was designed to be randomly controlled. Block randomization method was used to determine the experimental and control groups. Randomization was done by a biostatistician outside the researcher. 198 pregnant women were randomly assigned to the date fruit, nipple and control groups. From the 37th gestational age to the onset of labor, 6 date fruits were consumed per day by the date fruit group and the nipple stimulation was applied 6 minutes per day for the nipple group. No intervention was made for the control group. For the collection of research data, Structured Information Form and Wijma Birth Expectancy / Experience Scale Version were used.

Interventions

OTHERDate Fruit group

Consumption of Date Fruit

OTHERNipple group

Nipple Stimulation

Sponsors

Selcuk University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

The study was designed to be randomly controlled.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Women who nulliparous at the 37th gestational age, have singleton pregnancy, have the BMI is less than 25 kg/m2, planning to have a normal vaginal delivery, have vertex presentation, a volunteer to participate in the study, no smoking in pregnancy and have moderate birth fear according to W-DEQ were included in the study.

Exclusion criteria

* Women who have risk pregnancy (such as preterm labor risk, preeclampsia eclampsia, premature rupture of membranes, placenta previa, gestational diabetes, fetal anomaly and chronic diseases) were excluded in the study.

Design outcomes

Primary

MeasureTime frameDescription
The spontaneous onset of laborFrom the 37th gestational age to the laborThe spontaneous onset of labor (dichotomous data: yes or no)
Induction and augmentation of laborFrom the 37th gestational age to the laborInduction and augmentation of labor (dichotomous data: yes or no)

Secondary

MeasureTime frameDescription
Mode of deliveryFrom the 37th gestational age to the birthMode of delivery (dichotomous data: vaginal delivery or caesarean section)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026