Effect of light pressure stroking massage with placebo, sesame (Sesamum indicum) oil and olive oil on pain severity and amount of received analgesic in patients with trauma

Comparison the effect of light pressure stroking massage with placebo, with sesame (Sesamum indicum) oil and olive oil on pain severity and amount of received analgesic in patients with upper or lower limbs trauma

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015082814251N4

Enrollment

Registered

2015-09-19

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

Pain. Acute pain

Interventions

Intervention 1: We will ask patients in first intervention group to message trauma site for 5 minutes through light pressure stroking method with olive oil. Intervention 2: We will ask patients in sec

We will ask patients in first intervention group to message trauma site for 5 minutes through light pressure stroking method with olive oil.

We will ask patients in second intervention group to message trauma site for 5 minutes through light pressure stroking method with sesame (Sesamum indicum) oil.

We will ask patients in control group to message trauma site with placebo for 5 minutes through light pressure stroking method.

Eligibility

Sex/Gender

All

Age

15 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age range of 15-50 years old; full consciousness and being able to read and write, passing at least 1 hours and at last 6 hours from trauma; lack of infection, bone fractures, dislocation, amputation, nerve damage, presence of a foreign body and internal or external bleeding; lack of cast or splint at trauma site, having appropriate perfusion in trauma site; free from diabetes, cardiovascular, musculoskeletal diseases and peptic ulcers; not receiving anti-coagulant drugs in 3 months ago; lack of sensitivity or allergy to the oils plant group; lack of addiction and cigarette smoking; having moderate pain during arrival time (obtaining score between 3-6 based on visual analog scale). Exclusion criteria: refusing to referral to recruitment centers for follow up more than two times consecutively; any sing of allergy and complication in patients during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: At first, third, sixth and ninth days of intervention. Method of measurement: Pain assessment scale.	—

Secondary

Measure	Time frame
Amount of received analgesic. Timepoint: At first, third, sixth and ninth days of intervention. Method of measurement: Pain assessment checklist.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Farsi

Faculty of Nursing, Aja University of Medical Sciences, Tehran, Iran.

zahrafarsi@gmail.com+98 21 8833 7920

Outcome results

None listed

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