Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT05858255

Hjernegym - Effects of Exergaming in Psychosis: a Clinical Intervention Study

Led by Sykehuset i Vestfold HF · Updated on 2023-05-15

48

Participants Needed

1

Research Sites

196 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical intervention study is to investigate the effects of exergaming on cognition and other clinical symptoms in outpatient individuals with schizophrenia. The main questions it aims to answer are: Will an exergaming intervention contribute to improved cognition and reduced clinical symptoms, as well as enhanced physical health/self-efficacy/quality of life, in individuals with schizophrenia? Will the gaming component strengthen motivation for a physically more intensive component, so that attendance will be at least as high as in comparable exercise studies despite the current study being implemented in a resource-limited, regular clinical outpatient setting? Participants will be asked to engage in two 45 minutes exergaming sessions with a designated personal trainer for 12 weeks. Results pre- and post intervention will be compared, and comparisons will also be made with a former randomized controlled trial conducted at the same site, in which the currently combined activities were investigated separately (high-intensity interval training and low-intensity video gaming), both yielding positive but different effects.

CONDITIONS

Official Title

Hjernegym - Effects of Exergaming in Psychosis: a Clinical Intervention Study

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability to give consent
  • Understanding and speaking a Scandinavian language
  • Diagnosed with schizophrenia spectrum disorder (schizophrenia, schizoaffective disorder, or schizophreniform disorder) according to ICD-10 criteria
Not Eligible

You will not qualify if you...

  • Diagnosis of intellectual disability
  • Diagnosis of neurological disorder
  • History of severe head trauma
  • Pregnancy
  • Chest pain during exercise
  • Unstable angina pectoris
  • Malignant hypertension
  • Uncontrollable arrhythmia
  • Recent myocardial infarction
  • Acute infection with lymphadenopathy
  • Any other medical condition that makes participation unsafe

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

DPS Vestfold, Vestfold Sykehus HF

Tønsberg, Vestfold, Norway, 3120

Actively Recruiting

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Research Team

T

Tom Langerud Holmen, PhD

CONTACT

O

Ole Jakob Bredrup, MA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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