Positive Psychological Intervention for Parkinson's Disease Patients

Wenzhou Medical University

Status: Completed

Conditions: Parkinson

Treatments: Behavioral: Routine nursing methods; Behavioral: PERMA positive psychological intervention mode

Study type: Interventional

Funder types: Other

Identifiers

NCT06832358

Meichun Shu2

Details and patient eligibility

About

This study aims to evaluate the impact of positive psychological intervention based on the PERMA model on Parkinson's disease patients by assessing their depression, quality of life, and related psychological indicators before and after intervention.

Enrollment: 60 patients

Sex: All

Ages: 42 to 81 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subjects must meet the clinical diagnostic criteria for primary Parkinson's disease
• Subjects must not have a history of depression or other significant illnesses (e.g., stroke, coronary heart and tumor disease)
• Subjects should have clear consciousness, effective communication capabilities, and basic comprehension and reading skills to complete routine assessments
• The diagnosis of depression adhered to the ' Chinese Classification and Diagnostic Criteria for Mental Disorders ' (Revised Third Edition)
• Subjectsshould not have schizophrenia
• Subjects should not have substance abuse (alcohol, tobacco or other psychoactive substances)

Exclusion criteria

• Subjects with significant mental or cognitive impairment that communication or completion of scale assessments
• Subjects exhibiting severe self-harm or suicidal tendencies
• Subjects with severe dysfunction of the heart, liver, kidney or other critical organs
• Subjects with contraindications for transcranial magnetic stimulation (such as cochlear implant, pacemaker, built-in pump, artificial metal heart valve, suspected metal in the eye or elevated intracranial pressure)
• Subjects with a history of epilepsy that is poorly controlled
• Subjects with Parkinson's disease who have undergone surgical treatment

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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60 participants in 2 patient groups

Study group

Experimental group

Description:

The study group was treated with routine nursing combined with PERMA positive psychological intervention mode

Treatment:

Behavioral: PERMA positive psychological intervention mode

Behavioral: Routine nursing methods

Control group

Active Comparator group

Description:

The control group will receive routine nursing methods to ensure that patients receive standard medical support and treatment during the intervention period.

Treatment:

Behavioral: Routine nursing methods