Insomnia
Conditions
Interventions
Intervention group:The Magpro-100 magnetic stimulator made in Denmark was used, with a circular magnetic stimulation coil with a diameter of 12 cm and a maximum stimulation intensity of 2.0 T. Before
Sham stimulation group:The magnetic stimulation site was the same as the sham stimulation group, but the magnetic stimulation coil was perpendicular to the skull surface of the subjects, so the magnet
Sponsors
Military psychology departemnt, the Army Medical University, PLA
Eligibility
Sex/Gender
All
Age
18 Years to 25 Years
Inclusion criteria
Inclusion criteria: Crossover study: (1) The subjects were local undergraduate students in our university; (2) Recent good health and no definite physical or mental diseases that may affect sleep within 6 months; (3) Not taking any drugs that may affect sleep in the past 3 months; (4) Voluntarily participate in the trial and check the informed consent Intervention study: (1) The subjects were local undergraduate students in our university; (2) recent good health and no definite physical or mental diseases that may affect sleep within 6 months; (3) not taking any drugs that may affect sleep in the past 3 months; (4)ISI =15 and PSQI=8; (5) Patients voluntarily participated in this trial and signed informed consent.
Exclusion criteria
Exclusion criteria: Crossover study: (1) Non-college students or military students; (2) There was a history of epilepsy and/or family history, convulsion history, craniocerebral trauma history, syncope history, stroke history, brain tumor history, traumatic brain injury history, and no implantable medical devices in the body; (3) Physical and mental diseases (such as traumatic surgery, depressive disorder, schizophrenia, etc.) that may affect sleep in the past six months; (4) Taking substances that may affect sleep (e.g., melatonin, non-benzodiazepines, etc.) within the past 3 months; (5) Unable to cooperate with the completion of this trial. Intervention study: (1) Non-college students or military students; (2) There was a history of epilepsy and/or family history, convulsion history, craniocerebral trauma history, syncope history, stroke history, brain tumor history, traumatic brain injury history, and no implantable medical devices in the body; (3) physical and mental diseases (such as traumatic surgery, depressive disorder, schizophrenia, etc.) that may affect sleep in the past six months; (4) taking substances that may affect sleep (e.g., melatonin, non-benzodiazepines, etc.) within the past 3 months; (5)ISI <15 or PSQI <8; (6) Unable to cooperate with the completion of this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Computerized behavioral task(Color-word intervention task);computerized behavioral task(Color-word intervention task);Questionnaires(Cognitive flexibility index); | — |
Secondary
| Measure | Time frame |
|---|---|
| Questionnaires(Pittsburgh Sleep Quality Index);Questionnaires(Insomnia severity index); | — |
Countries
China
Contacts
Public ContactLi Peng
Military psychology departemnt, the Army Medical University, PLA
Outcome results
None listed