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the effect of foot reflexology massage on fatigue and anxiety

Effectiveness of foot reflexology on fatigue and anxiety after cesarean section in mothers with hospitalized preterm neonate in Neonatal Intensive Care Unit(NICU)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201203229322N1
Enrollment
99
Registered
2012-06-30
Start date
2012-09-22
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

Condition 1: fatigue. Condition 2: anxiety. Other specified neurotic disorders Generalized anxiety disorder

Interventions

Intervention 1: "Foot reflexology massage" or "reflexology" iwill be done for the intervention group which include three stages: preparation, heating with a 15-step techniques and massage techniques o
Placebo
"Foot reflexology massage" or "reflexology" iwill be done for the intervention group which include three stages: preparation, heating with a 15-step techniques and massage techniques on reflex points
The intervention in the placebo group includes the preparation and heating with a towel and massage the legs and it is done within three consecutive days and takes 40 minutes for both legs (20 minute
In the control group, no intervention will be applied. This group will only receive routine care.

Sponsors

Vice chancellor for research Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Nulliparous mothers with cesarean section and hospitalized for three full days ; mothers with the age of 20-35 years old; mothers should be literate; mothers with no serious physical and psychological disorders; mothers with no tissue damage on their feet; mothers with gestational age of 30-37 weeks; mothers with preterm neonate hospitalized in NICU; the newborns have to be breastfed. Exclusion criteria: -mothers with no willingness to participate in the trial anymore; mothers with less than three full days hospitalization; mothers who will develop serious health conditions during the trial; mothers who will develop a tissue damage on their feet, during the intervention; mothers who give birth with gestational age of less than 30 weeks; initiating formula feeding in the neonates, for any reasons.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety intensity. Timepoint: pre and post intervention (before the initiation of first intervention and after the 3rd day of intervention). Method of measurement: Spielberger State Anxiety Inventory.;Fatigue intensity. Timepoint: pre and post intervention (before the initiation of first intervention and after the 3rd day of intervention). Method of measurement: visual analoge scale for fatigue.

Secondary

MeasureTime frame
Pulse. Timepoint: Once before and once after the third day of intervention and within 10 minutes afte intrventionr. Method of measurement: According to minutes using the standard digital clock.;Blood pressure. Timepoint: Once before and once after the third day of intervention and within 10 minutes after intervention. Method of measurement: Mercury blood pressure devices (Richter).;Breathing. Timepoint: Once before and once after the third day of intervention and within 10 minutes afte intrvention. Method of measurement: According to minutes using the standard digital clock.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElalel Ruhi Rahim Begloo

Faculty of Nursing and Midwifery - Tehran University of Medical Sciences

fnm@sina.tums.ac.ir e-ruhi@razi.tums.ac.ir+98 21 6693 3600

Outcome results

None listed

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