Feasibility and Relevance of High-Intensity Functional Training in Patients With First-Episode Psychosis

NCT03409393 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2018-09-14

No results posted yet for this study

Summary

The aim of the COPUS study is to investigate, whether it is possible to recruit and retain young people with first-episode psychosis, to an 8 week supervised High-Intensity Functional Training intervention (HIFT) (i.e. COPUS Intervention) and to investigate if oxygen uptake, body composition and physical function improves following participation in the intervention.

Conditions

  • Schizophrenia
  • Schizotypal Disorder
  • First Episode Psychosis
  • Psychotic Disorders
  • Schizoaffective Disorder

Interventions

OTHER

The COPUS intervention

The COPUS intervention consists of 8 weeks of High-Intensity Functional Training (HIFT). The frequency of the training is 3 sessions per week and the duration is one hour per session. The intervention is group-based and supervised. Each training session includes warm-up (15 min), followed by 30 minutes of HIFT based on a range of varied functional exercises, including elements of strength training and aerobic exercise. The sessions are supervised by a trained physiotherapist and exercise physiologist supported by 2 two trained bachelor students in Sports Science.

OTHER

Usual Care (OPUS treatment)

Usual care include specialised early intervention treatment (OPUS treatment) and consists of three main pillars: modified assertive treatment, family involvement, and social skill training. OPUS treatment is delivered via multidisciplinary teams include psychiatrists, psychologists, nurses, social workers, physiotherapists, and vocational therapists. All team members, except for the psychiatrist, function as case managers. The ratio of patients to case managers must not exceed 12:1.

Sponsors & Collaborators

  • University of Copenhagen

    collaborator OTHER
  • Mental Health Services in the Capital Region, Denmark

    collaborator OTHER
  • Rigshospitalet, Denmark

    lead OTHER

Principal Investigators

  • Julie Midtgaard, Ph.D. · The University Hospitals Centre for Health Research (UCSF) / Copenhagen University Hospital (Rigshospitalet)

  • Helle Schnor, Ph.D. · Mental health services in the Capital Region of Denmark, Psychiatric Center Glostrup

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-22
Primary Completion
2018-06-20
Completion
2018-08-01

Countries

  • Denmark

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03409393 on ClinicalTrials.gov