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Effect of Reflexology Massage on Post operative Appendectomy pain

Effect of Reflexology Massage on Post operative Appendectomy pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013122615946N1
Enrollment
105
Registered
2014-05-28
Start date
2013-12-06
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

Appendectomy. Acute appendicitis with localized peritonitis

Interventions

Intervention 1: In intervention group pain intensity was recorded, then the patient's right leg in a certain area was pressed by the therapist who has been trained by a specialist for ten minutes by a
Treatment - Other
Placebo
In intervention group pain intensity was recorded, then the patient's right leg in a certain area was pressed by the therapist who has been trained by a specialist for ten minutes by a special mean (s
Patients in the placebo group had a pressure point on the back of the left leg that was pressed with less intensity. ear seed was attached to the left earlobe of a patient without compression balls an

Sponsors

Sabzevar University of Medical Siences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: inclusion criteria : age between 15 to 60, the diagnosis of appendicitis, appendectomy by a single surgeon and full consciousness. exclusion criteria: Previous surgery, addiction, emotional disorders, diabetes, mental disorders, age below 15 years and above 60 years of age, spinal anesthesia, the patient's unwillingness to participate in the study, history of reflexology massage, having chronic pain in other body regions, sensitivity to touch or massage, having fever and skin diseases, pregnancy, severe complications after the surgery, a member of the feet and hands health disorders, hearing disorders and get home before the intervention

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before intervention, 0, 1, 6 and 24 hours after itervention. Method of measurement: 0-10 visual analog scale.

Secondary

MeasureTime frame
Sedative consumptin. Timepoint: before intervention, 0, 1, 6 and 24 hours after itervention. Method of measurement: Review patient file.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Baghani

Sabzevar University of Medical Sciences

baghani_sara@yahoo.com; baghanis2@mums.ac.ir+98 51 1609 1195

Outcome results

None listed

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