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Comparing The Effect Of Single and Combined Nature Based-Sound and Foot Reflexology On Level Of Consciousness And Physiological Indicatores Of Traumatic Comatose Patients

Comparing The Effect Of Single And Combined Nature Based-Sound and Foot Reflexology On Level Of Consciousness And Physiological Indicatores Of Traumatic Comatose Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015120125339N1
Enrollment
120
Registered
2016-05-13
Start date
2016-02-09
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

Trumatic Comatoes Patient. Injuries to the head

Interventions

Intervention 1: Intervention 1: In the intervention group with sounds of nature, patients will listen to nature sounds through headphones twice a day for 30 minutes each morning and evening for 14 day
Rehabilitation
Intervention 3: In the intervention group with foot reflexology and nature sound,patients will receive both intervention( nature sound and foot reflexology) twice a day for 30 minutes each morning
Control group: in The control group,patients will not receive any interventions.
Intervention 1: In the intervention group with sounds of nature, patients will listen to nature sounds through headphones twice a day for 30 minutes each morning and evening for 14 days
Intervention 2: In the intervention group with foot reflexology massag,foot reflexology massag will do for patients twice a day for 30 minutes each morning and evening for14 days,

Sponsors

Vice Chancellor for Research, Iran University Of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria include : Age Between 15 to 75 Years;Traumatic Comatose Patients with GCS Less Than 8;24 to 72 Hours After Admision At ICU;Lack of any brain injur;Lack of Hearing Impairment; ;Lack of Diabet And Arrhythmia;Lack of History Of Downing;Patients Undergoing Craniotomy and Propofol Will Be Enrolled In the Study 24 Hours After Craniotomy. Exclusion Criteria Include: Patients Who Do Not Tolerate The Procedure; If They Will Undergo Rapid Changes In Vital Signs ,Tachycardia( Heart Rate More Than 120), respiratory distress(Respiratory Rate More Than 24 Per Minute) Will Be Excluded From The Study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Level of consiosness. Timepoint: before intervention,one and two weeks after intervention. Method of measurement: glasco coma scale.

Secondary

MeasureTime frame
Physiological Indicatores. Timepoint: Physiological Indicatores will be measured during 5 to 10 minutes before intervention, immediately after the intervention, 25 to 30 minutes after the intervention, 2 hours after intervention. Method of measurement: Check List.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElahe Bahonar

School of Nursing & Midwifery of Iran University

e.bahonar2235@gmail.com+98 21 8888 2886

Outcome results

None listed

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