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The effect of sensory stimulation on the vital signs and level of consciousness of concussion patients

The effect of multifaceted sensory stimulation on arterial blood oxygen, heart rate, blood pressure and level of consciousness of concussion patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230225057521N1
Enrollment
64
Registered
2024-08-12
Start date
2022-07-07
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Concussion patients. Concussion

Interventions

Intervention 1: Intervention group: The intervention consists of a regular and periodic program of sensory stimulation for 6 days, each session lasting a maximum of 30 minutes in the morning (8 am) an

Sponsors

Zabol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
11 Years to 65 Years

Inclusion criteria

Inclusion criteria: The patient does not have a history of sensory disorders in the upper limbs, and patients without sensory disorders are included in the study according to the doctor's opinion. Don't have a diagnosis of an underlying disease such as diabetes (due to possible neuropathies based on the patient's file). The patient has been admitted to the ward with a diagnosis of concussion. Concussion includes subdural, epidural, intracerebral, ventricular, and subarachnoid hemorrhages. The level of consciousness of the patient should be in the range of 8 to 10 (according to the Glasgow Coma Scale). The patient's age should be between 65 and 11 years. Filling out the written informed consent by the guardians

Exclusion criteria

Exclusion criteria: The simultaneous participation of the patient in similar care programs such as massage therapy and the use of relaxation techniques and... History of previous brain injury Fractures in four limbs (arms and legs)

Design outcomes

Primary

MeasureTime frame
Arterial blood oxygen level. Timepoint: Measurement of arterial blood oxygen level in 6 days, 4 times a day, in the morning and evening, before and after the intervention. Method of measurement: Pulse oximetry device.;Number of heartbeats. Timepoint: Measurement of heart rate in 6 days 4 times a day in two times in the morning and in the evening before and after the intervention. Method of measurement: Pulse oximetry device.;Blood pressure (systolic and diastolic). Timepoint: Measurement of blood pressure (systolic and diastolic) in 6 days, 4 times a day, in the morning and evening, before and after the intervention. Method of measurement: Sphygmomanometer and stethoscope.;Level of consciousness. Timepoint: Measuring the level of consciousness in 6 days, 4 times a day, twice in the morning and in the evening, before and after the intervention. Method of measurement: Glasgow coma scale chart.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactYaser Moshtaghi

Zabol University of Medical Sciences

y.moshtaghi18@gmail.com+98 54 3222 4708

Outcome results

None listed

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