Effects of psychological interventions on pain, anxiety, and physiological parameters in patients with cerebral stroke

?Evaluating the effects of psychological interventions on pain, anxiety and physiological parameters in the patients with cerebral stroke hospitalized in the intensive care unit: a parallel randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180711040432N4

Enrollment

Registered

2020-12-30

Start date

2020-11-10

Completion date

Unknown

Last updated

2021-01-05

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

Conditions

Cerebral stroke. Cerebellar stroke syndrome

Interventions

Intervention 1: Control group: In the control group, patients will receive only the usual care of the department (these include: physician's examination, daily drug therapy, serum therapy). Interventi

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Consciousness level based on the Glasgow Coma Index (GCS) greater than 9 ?The diagnosis of hemorrhagic or ischemic cerebral stroke The age of 18 to 75 years

Exclusion criteria

Exclusion criteria: The death of patient during the study The exacerbation of stroke during the study

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: Before the start of intervention at the first session and after the end of intervention at the last session. Method of measurement: VAS questionnaire.;Anxiety. Timepoint: Before the start of intervention at the first session and after the end of intervention at the last session. Method of measurement: VAS questionnaire.;Changes of the physiological parameters of patients with cerebral stroke. Timepoint: Before the start of intervention at the first session and after the end of intervention at the last session. Method of measurement: The monitor used in the intensive care unit and a mercury thermometer.	—

Measure

Time frame

Pain. Timepoint: Before the start of intervention at the first session and after the end of intervention at the last session. Method of measurement: VAS questionnaire.;Anxiety. Timepoint: Before the start of intervention at the first session and after the end of intervention at the last session. Method of measurement: VAS questionnaire.;Changes of the physiological parameters of patients with cerebral stroke. Timepoint: Before the start of intervention at the first session and after the end of intervention at the last session. Method of measurement: The monitor used in the intensive care unit and a mercury thermometer.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Mohammadpourhodki

Mashhad University of Medical Sciences

rezamdpoor@gmail.com+98 51 5525 4590

Outcome results

None listed

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