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The effect of foot reflexology on labor outcome

The effect of foot reflexology on anxiety, pain and outcomes of labor in primiparus woman referred to the Karaj hospital in 2011

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103015948N1
Enrollment
50
Registered
2011-06-24
Start date
2011-06-08
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Labor outcomes. Delivery

Interventions

Intervention 1: For intervention group: Gentle massage of all surface of plantar and some points upon of feet using thumb and pointing fingers then continuous pressure on solar network, pituitary and
For intervention group: Gentle massage of all surface of plantar and some points upon of feet using thumb and pointing fingers then continuous pressure on solar network, pituitary and uterus points i
For control group: Receiving routine care of labor ward and massages of other parts of foot except three main points that mentioned, for 40 minutes (20 minutes per foot) at 3-4 cm dilatation.

Sponsors

Vice chancellor for research, Islamic Azad University of Karaj branch
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Women with singleton pregnancies and fetal with cephalic presentation, gestational age 37-41 weeks, without active psychiatric disorders and anxiety on personality according to Beck and Spielberger questionnaires, without mental retardation, blindness and deafness, absence of fever, seizures, thrombosis, renal or gallbladder stones, foot disease, swelling, ulcer, trauma and fractures in the foot, not using the anti-anxiety medications and methods of complementary medicine during the previous week. Exclusion criteria: Use of any drug or method of analgesia and anesthesia, induction of labor with Oxytocin, abnormal fetal heart patterns, presence of any special medical condition (e.g. chronic diseases) and nature of taking any drug, women with a history of abortion, gestational hypertension, presence of any abnormal bleeding from placental abruption or placenta previa, polyhydroamnious, oligohydroamnious and intrauterine growth restriction that proved by ultrasound method, passing more than 12 hours from the time of rupture of membrane.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Labor pain intensity. Timepoint: Before intervention in 3-4cm cervical dilatation and immediately, half, one and two hours after the intervention. Method of measurement: McGill pain questionnaire.;Anxiety score. Timepoint: Before intervention in 3-4cm cervical dilatation and immediately after the intervention. Method of measurement: Spielberger anxiety inventory.;Duration of the first stage of labor. Timepoint: One time the start of labor until complete effacement and cervical dilatation. Method of measurement: According to minutes using the standard digital clock.;Duration of the second stage of labor. Timepoint: One time from full dilatation of cervix to departure of baby. Method of measurement: According to minutes using the standard digital clock.;Duration of the third stage of labor. Timepoint: One time from departure of baby to complete withdrawal of placenta. Method of measurement: According to minutes using the standard digital clock.

Secondary

MeasureTime frame
Type of delivery. Timepoint: One time after departure of baby. Method of measurement: Observed as a vaginal delivery, instrumental delivery and cesarean section.;Apgar score. Timepoint: At 1 and 5 minutes after birth. Method of measurement: Observation and examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoheila Moghimi Hanjani

Islamic Azad University Karaj branch

soheila.moghimi@kiau.ac.ir;somoghimi@yahoo.com+98 21 7720 4224

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026