MedPath

Exercise and Overnight Motor Sequence Task

Not Applicable
Completed
Conditions
Schizophrenia and Related Disorders
Psychotic Disorders
Registration Number
NCT03800368
Lead Sponsor
The University of Hong Kong
Brief Summary

The objective of this randomized controlled trial (RCT) is to compare the changes of the sleep-related memory functions in patients with psychosis after they have completed the 12-week high-intensity exercise intervention, the 12-week low-intensity exercise intervention, or the 12-week controlled non-exercise intervention respectively. Fifty-one patients with psychosis, patients who received either the high-intensity exercise or low-intensity exercise as intervention shown a significant improvement to their impaired sleep-related memory function, while those who received non-exercise intervention has no such improvement. Moreover, high-intensity exercise may have a more prominent effect compare to low-intensity exercise.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
51
Inclusion Criteria
  • Aged from 18 to 55
  • Based on the SCID diagnosed to have schizophrenia and related psychotic disorders
  • Ability to understand the nature of the study and to give written informed consent
Exclusion Criteria
  • Severe physical illness (Myocardial Infarction, Hypertension, Fracture, Spinal problems in which exercise may be contraindicated), and seizure disorders
  • Comorbid substance dependence
  • Unstable psychotic symptoms
  • A history of brain trauma or organic brain disease
  • Known history of intellectual disability or special school attendance
  • Answered one or more "yes" in the PAR-Q and without doctors approval for exercise

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
The sleep-dependent procedural memory consolidation after 12 weeks of intervention12-week Follow-up

Tested by comparing the finger-tapping motor sequence task performance between the three groups during the 12-week follow-up assessment.

Secondary Outcome Measures
NameTimeMethod
The verbal memory consolidation after 12 weeks of intervention12-week Follow-up

Tested by comparing the logical memory task performance between the three groups during the 12-week follow-up assessment

The sleep quality after 12 weeks of intervention12-week Follow-up

Measured by using the Pittsburgh Sleep Quality Index (PSQI) and compare the differences between the three groups during the 12-week follow-up assessment

The insomnia severity after 12 weeks of intervention12-week Follow-up

Measured by using the Insomnia Severity Index (ISI) and compare the differences between the three groups during the 12-week follow-up assessment

The attention performance after 12 weeks of intervention12-week Follow-up

Measured by using the cancellation task performance and compare between the three groups during the 12-week follow-up assessment

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.