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The effectiveness of tactile stimulation on unconscious patients

The effectiveness of tactile stimulation on level of consciousness, pain, and physiological parameters in unconscious patients admitted to the intensive care

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110912007529N22
Enrollment
90
Registered
2020-03-29
Start date
2019-08-21
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

comatose patient. Coma, unspecified

Interventions

Intervention 1: The first intervention group:The hand tactile stimulation group receive touch for 10 minutes, twice a day,11:00 am and 15:00 pm, for three days. Intervention 2: The second intervention

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age range 18 to 60 years old The level of consciousness based on Glasgow coma scale is less than 12 The Richmond criteria in the range of 3- to 3+ Existence of pain in patients by CPOT criteria Existence of normal brain CT Hospitalization in ICU for the first time The lack of history of mental illness The lack of addiction The lack of sensory-motor dysfunction in the extremities The lack of skin problems The lack of diseases such as diabetes

Exclusion criteria

Exclusion criteria: Concurrent participation in similar care plans such as massage Use of receive neuromuscular blockers Severe disorders levels of consciousness

Design outcomes

Primary

MeasureTime frame
Level of consciousness. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: The GCS and FOUR scores.;Intensity of pain. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: Critical Care Pain Observation Tool (CPOT).

Secondary

MeasureTime frame
Blood Pressure. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: The monitor used in Intensive Care Unit.;Respiratory Rate. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: The monitor used in Intensive Care Unit.;Heart Rate. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: The monitor used in Intensive Care Unit.;Oxygen Saturation. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: Pulse Oximeter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNahid Rejeh

Shahed University

nrejeh@yahoo.com+98 21 2150 5121

Outcome results

None listed

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