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The effect of tactile stimulation on vital signs and consciousness of traumatic brain injury patients hospitalized in intensive care units

The effect of tactile stimulation on vital signs and consciousness of traumatic brain injury patients hospitalized in intensive care units

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016062128563N1
Enrollment
60
Registered
2017-06-09
Start date
2016-11-02
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

head trauma Patients. Injuries to the head

Interventions

Intervention 1: Intervention group: Intervention in this case would be The intervention group, touch the wrist and the whole hand For 5 minutes, In the morning and evening for control group, all the
Treatment - Devices
Intervention group: Intervention in this case would be The intervention group, touch the wrist and the whole hand For 5 minutes, In the morning and evening for control group, all the routine cares w
Control group:the control group, vital signs twice a day (at 11 am and 5 evenings) with an interval of 5 minutes, while rejecting any intervention on the patient.

Sponsors

Vice chancellor for research of Qazvin university of medical science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The patient is hospitalized with a diagnosis of head trauma; Patient age ranged from 18 to 65 years; diagnosis of underlying disease such as diabetes (neuropathy due to possible based on patient records) is not; upper limb disorders in no sense; upper limb disorders in no sense; The patient's level of consciousness is in the range of 5 to 8; patient mental problems such as hallucinations or have anxiety disorders Exclusion criteria:patient dissatisfaction partners to continue to participate in the study; sample transport to other centers outside the city of Qazvin; a sharp drop in the level of consciousness suddenly; patients in both groups during the study and control at the same time patient care plans similar companies such as massage and relaxation techniques

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Level of consciousness. Timepoint: Before and after the intervention. Method of measurement: Using the Glasgow Coma Scale.

Secondary

MeasureTime frame
Vital sign. Timepoint: Before and after the intervention. Method of measurement: Using the monitoring -barometer-digital thermometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Leily Yekeh fallah

Qazvin University of Medical Sciences

info@qums.ac.ir+98 283336001

Outcome results

None listed

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