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Comparison of the effect of ear acupressure and foot reflexology on pain and anxiety in women following elective cesarean section

Comparison of the effect of foot reflexology and Auriculotherapy on pain and anxiety in women following elective cesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014122920475N1
Enrollment
132
Registered
2015-11-06
Start date
2015-09-23
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

Cesarean pain and anxiety. single delivery by caesarean section

Interventions

Intervention 1: foot reflexology prformed in the first intervention group. Reflexology intervention performed once for 20 minutes in both legs 2-3 hours after injecting anesthetic for spinal anest
Behavior
foot reflexology prformed in the first intervention group. Reflexology intervention performed once for 20 minutes in both legs 2-3 hours after injecting anesthetic for spinal anesthesia.
in the second intervention group Auriculotherapy performed once for 20 minutes in both ears.

Sponsors

Mashhad Univercity of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: inclusion criteria include singleton pregnancy; gestational age more than 37 weeks; Labor pains not start; The elective cesarean section planned before the onset of labor; using Spinal analgesia for caesarean section; No Medical condition in mother (cardiac, respiratory, hepatic or neurologic); normal body mass index (18.5< BMI <30) in first trimester of pregnancy; lack of injuries and wounds at the feet or ears; no history of migraine; no History of foot reflexology or Auriculotherapy; No addiction to drugs, sedatives and alcohol in mother. Exclusion criteria: uncomfortable feel in ear acupressure or foot massage; Lack of cooperation from the study; the cesarean incision is not transverse; complications during and after surgery such as excessive bleeding , adhesions, fetal death and prolonged duration of surgery(more than 1 hour).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 2-3Hours after anesthetic injection - 2 and 3 hours after Intervention. Method of measurement: McGill pain questionnaire-Visual Analogue Scale.;Anxiety. Timepoint: 3-2 hours after injection of anesthetic- One and two hours after the intervention. Method of measurement: Anxiety Inventory Spielberger.

Secondary

MeasureTime frame
Nausea -Bloodshed. Timepoint: One and two hours after the intervention. Method of measurement: Nausea visual analogue scale.;Bloodshed. Timepoint: One and two hours after the intervention. Method of measurement: Weighing pads soaked in blood.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMousavi Fatemeh sadat

Mashhad University of Medical Sciences

mousavif922@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

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