The effect of lavender aromatherapy on maternal somatic pain, fatigue and mood in the early hours after delivery admitted

The effect of lavender aromatherapy on maternal somatic pain, fatigue and mood in the early hours after delivery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014060910327N7

Enrollment

Registered

2014-07-01

Start date

2014-04-06

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

Relationship of lavender aromatherapy on maternal somatic pain, fatigue and mood in the early hours after delivery.

Interventions

Intervention 1: Intervention group: Essential oil of lavender (1%) based on sesame oil was used in case group. Five drop of essence squeezed on 3 layers of kleenex and participants hold it in 20 cm o

Treatment - Drugs

Intervention group: Essential oil of lavender (1%) based on sesame oil was used in case group. Five drop of essence squeezed on 3 layers of kleenex and participants hold it in 20 cm of their noses fo

control group: In the control group used sesame oil. Five drop of essence squeezed on 3 layers of kleenex and participants hold it in 20 cm of their noses for 15 minutes and do respiration. Then in t

Eligibility

Sex/Gender

Female

Age

18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Nulliparous; natural vaginal delivery; Age between 18 to 35 years; by episiotomy Exclusion criteria: allergic to Lavender

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Prineal pain. Timepoint: One to four hours after delivery. Method of measurement: Visual Analog Scale for pain.;Fatigue. Timepoint: One to four hours after delivery. Method of measurement: Visual Analog Scale for fatigue.;Physical pain. Timepoint: One to four hours after delivery. Method of measurement: Visual Analog Scale.;Mood. Timepoint: One to four hours after delivery. Method of measurement: Positive And Negative Affect Scale (PANAS).	—

Measure

Time frame

Prineal pain. Timepoint: One to four hours after delivery. Method of measurement: Visual Analog Scale for pain.;Fatigue. Timepoint: One to four hours after delivery. Method of measurement: Visual Analog Scale for fatigue.;Physical pain. Timepoint: One to four hours after delivery. Method of measurement: Visual Analog Scale.;Mood. Timepoint: One to four hours after delivery. Method of measurement: Positive And Negative Affect Scale (PANAS).

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Secondary

Measure	Time frame
Prineal pain. Timepoint: Before, One hours after the first intervention, In the morning after the intervention. Method of measurement: Visual Analog Scale.;Fatigue. Timepoint: Before, One hours after the first intervention, In the morning after the intervention. Method of measurement: Visual Analog Scale for fatigue.;Physical pain. Timepoint: Before, One hours after the first intervention, In the morning after the intervention. Method of measurement: Visual Analog Scale.;Mood. Timepoint: Before, One hours after the first intervention, In the morning after the intervention. Method of measurement: Positive And Negative Affect Scale (PANAS).	—

Measure

Time frame

Prineal pain. Timepoint: Before, One hours after the first intervention, In the morning after the intervention. Method of measurement: Visual Analog Scale.;Fatigue. Timepoint: Before, One hours after the first intervention, In the morning after the intervention. Method of measurement: Visual Analog Scale for fatigue.;Physical pain. Timepoint: Before, One hours after the first intervention, In the morning after the intervention. Method of measurement: Visual Analog Scale.;Mood. Timepoint: Before, One hours after the first intervention, In the morning after the intervention. Method of measurement: Positive And Negative Affect Scale (PANAS).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarideh Vaziri

Faculty of Nursing and Midwifery

Vazirif@sums.ac.ir+98 71 1647 4252

Outcome results

None listed

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