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The effect of massage with clove oil on pain and anxiety caused by IT/LP

The effect of effleurage massage with clove oil on IT/LP pain and anxiety among children with cancer: A randomized clinical trial.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230428058019N1
Enrollment
39
Registered
2023-05-25
Start date
2023-05-07
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

cancer. Multiple myeloma and malignant plasma cell neoplasms

Interventions

Intervention 1: Intervention group: Intervention group: 1 Working method in intervention group 1 (Effleurage massage group with clove oil) In addition to receiving routine care, this group received e

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 11 Years

Inclusion criteria

Inclusion criteria: Definitive diagnosis of cancer and hospitalization in the ward . Prescribing LP and receiving IT Children aged 7 to 11 years

Exclusion criteria

Exclusion criteria: 1. The order to receive midazolam or other sedatives before the procedure 2. The child's restlessness and intolerance of research conditions 3. Loss of consciousness and lack of awareness of time, place and person 4. Severely ill and end-stage child 5. The need to observe contact precautions 6. Fever, risk of bleeding (platelet count less than 20,000), leukopenia 7. Inability to communicate verbally (deafness) and vision disorders and physical defects, Down's syndrome and genetic diseases that disrupt the expression and experience of pain. Having a wound, fracture, infection, redness and abnormal swelling in the massage area 8. People undergoing IT/LP for the first time. History of allergy to clove and sweet almond oil

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: The pain variable will be evaluated 20 minutes before the intervention and 3 minutes after the intervention. Method of measurement: visual analog scale of pain.;Anxiety. Timepoint: The anxiety variable will be evaluated 20 minutes before the intervention and 3 minutes after the intervention. Method of measurement: Children’s Anxiety Meter-Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeila Valizadeh

Tabriz University of Medical Sciences

fatemehrahimi028@gmail.com+98 41 3477 0649

Outcome results

None listed

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