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comparison of two insomnia treatment protocols using transcranial direct current stimulation And its effects on cognitive functions and mood in women with chronic insomnia disorder

comparison of two insomnia treatment protocols using transcranial direct current stimulation And its effects on cognitive functions and mood in women with chronic insomnia disorder

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190620043954N2
Enrollment
48
Registered
2022-01-23
Start date
2022-01-15
Completion date
Unknown
Last updated
2022-02-07

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

Conditions

insomnia. Insomnia

Interventions

Intervention 1: Intervention group 1: Direct current of 2 mA will be applied for 20 to 30 minutes in 12 sessions (3 times a week). In this group, direct transcranial electrical excitation includes ano

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: female Ages 18 to 55 years Get a score of 15 to 28 in the Insomnia severity index Do not take sleeping pills or resist drug treatment despite taking the medication

Exclusion criteria

Exclusion criteria: Having a history of psychiatric neurological diseases (Alzheimer's, epilepsy, Parkinson's, mental retardation, etc.) and brain damage Drug abuse, alcohol or caffeine according to DSM5 diagnostic criteria Existence of bioelectric devices implanted in the body, such as a heart rate monitor Being pregnant Level of education less than diploma

Design outcomes

Primary

MeasureTime frame
In the present study, the primary outcome of the intervention is insomnia treatment, which is measured according to the difference of at least 10% between the pre-test and post-test scores of the participants in the scale of insomnia severity. Also, the evaluation of this outcome in the implementation of two different treatment protocols is evaluated according to the difference of at least 10% of the post-test scores of the participants' insomnia severity index. Timepoint: 1 to 5 days before the intervention and 1 to 5 days after the intervention. Method of measurement: Insomnia Severity Index.

Secondary

MeasureTime frame
Memory. Timepoint: 1 to 5 days before the intervention and 1 to 5 days after the intervention. Method of measurement: N-back Test.;Attention. Timepoint: 1 to 5 days before the intervention and 1 to 5 days after the intervention. Method of measurement: Stroop Test.;Problem Solving. Timepoint: 1 to 5 days before the intervention and 1 to 5 days after the intervention. Method of measurement: Wisconsin Card Sorting Test.;Mood. Timepoint: 1 to 5 days before the intervention and 1 to 5 days after the intervention. Method of measurement: Positive and Negative Affection Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahereh Motevalizadeh

Tehran University of Medical Sciences

tt.motevalli@gmail.com+98 21 6683 2371

Outcome results

None listed

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