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Acute stress persistence in ischemic stroke patients

comparison of Acute stress persistence in ischemic stroke patients with healthy patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171128037666N1
Enrollment
20
Registered
2018-06-02
Start date
2017-11-22
Completion date
Unknown
Last updated
2018-07-16

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

Conditions

chronic ischemic stroke. Cerebellar stroke syndrome

Interventions

Intervention 1: Intervention group: People with chronic stroke. Type of intervention: Stress which is generated by the TSST protocol. During this protocol, the person is initially interviewed for 2 mi

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The first inclusion criteria is the incidence of ischemic stroke should be 6 months to 3 years before the study, which approved by CT scan or MRI The Modified Ranking Scale for chronic stroke patients should be <= 3 The participants should not be disordered with systemic disorders like Diabetes, autoimmune disorders, cardiovascular disorders and neurological or psychiatric disorders. The participants should not have cigarette smoking at least one day before the study The participants should not have severe exercise at least one month before the study

Exclusion criteria

Exclusion criteria: Failure to cooperate in completing test procedures

Design outcomes

Primary

MeasureTime frame
Salivary cortisol levels before and after intervention. Timepoint: Salivary cortisol levels before intervention, immediately after intervention, twenty minutes after intervention and forty minutes after intervention. Method of measurement: The concentration of cortisol in the saliva samples measure in the laboratory by the salivary cortisol assay kit.

Secondary

MeasureTime frame
Linear and non-linear features of heart rate variation. Timepoint: linear and non-linear indicators of heart rate fluctuations as a secondary outcome, can be measured immediately before the TSST intervention, during the TSST protocol, twenty minutes after the end of the protocol, and forty minutes after the end of the protocol. Method of measurement: ECG instrument.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBoshra Hatef

Bagheiat-allah University of Medical Sciences

boshrahatef@bmsu.ac.ir+98 21 8804 0060

Outcome results

None listed

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