Various psychiatric disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients admitted to psychiatric care wards who give consent to participate in the study, can clearly express their wishes, and have a prescription for rehabilitation.
Exclusion criteria
Exclusion criteria: Individuals who meet any of the following criteria will be excluded from the study: Judged as unsuitable for participation by the attending physician. Inability to provide informed consent for the study. Severe hypertension (systolic blood pressure >= 200 mmHg or diastolic blood pressure >= 110 mmHg). Presence of an implanted pacemaker. History of epilepsy. Presence of sensory disorders or skin lesions at the stimulation site.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Knee extension strength at baseline (pre-intervention), 8 weeks, 12 weeks (end of intervention), and at 6-week follow-up. | — |
Secondary
| Measure | Time frame |
|---|---|
| The following outcomes assessed at baseline (pre-intervention), 12 weeks (end of intervention), and at 6-week follow-up: Quality of life assessed by the Sarcopenia Quality of Life (SarQoL) questionnaire Short Physical Performance Battery (SPPB) Neuropsychiatric Inventory-Questionnaire (NPI-Q) Medical Research Council (MRC) sum score | — |
Countries
Japan
Contacts
Nandan Senyo-kai Minamiawaji Hospital Rehabilitation Department