search
Back to results

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

Primary Purpose

Schizophrenia, Schizotypal Disorder, First Episode Psychosis

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
The COPUS intervention
Usual Care (OPUS treatment)
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Schizophrenia focused on measuring Human, Denmark, Adult, Adolescent, Young Adult, Male, Female, Physical Activity, Maximum Oxygen Consumption, Resistance Training, High-Intensity Functional Training, Aerobic Exercise, Motivation, Feasibility, Relevance, Health Behavior

Eligibility Criteria

18 Years - 35 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age between 18 and 35 years
  • Diagnosed with Schizophrenia or Schizotypal disorders
  • Undergoing OPUS treatment for at least 6 months or stabilized medical anti-psychotic treatment
  • Danish speaking

Exclusion Criteria:

  • Physical contraindications for physical activity
  • Pregnant (self-reported)
  • Unable to give adequately informed consent
  • Mentally disabled

Sites / Locations

  • OPUS

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Intervention Group

Control Group

Arm Description

The COPUS intervention plus usual care (OPUS treatment).

Usual care (OPUS treatment).

Outcomes

Primary Outcome Measures

Assessment of changes in Physical Fitness (VO2max)
Assessed by the maximum amount of oxygen the body can utilize during a specified period of intense exercise.
Recruitment Rate
Registration of patients enrolled in the study compared to the total number of eligible patients.
Retention Rate
Registration of the participants attendance in the High-Intensity Functional Training compared with the number of possible training sessions during the period.

Secondary Outcome Measures

Assessment of changes in body weight
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining body weight.
Assessment of changes in fat percentage
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining fat percentage.
Assessment of changes in bone mass
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining bone mass.
Assessment of changes in muscle mass
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining muscle mass.
Assessment of changes in Visceral Fat
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining visceral fat.
Assessment of changes in Resting Blood Pressure
The participants' Resting Blood Pressure are tested according to the American Heart Association practice guidelines for blood pressure Measurement.
Assessment of changes in countermovement jump height
Determination of potential changes in countermovement jump height measured using the non-invasive Optojump system (www.optojump.com)
Assessment of changes in Leg Muscle Strength
Determination of potential changes in leg muscle strength by the non-invasive 30-Second Chair Stand test. The test measures how many times the participant can reach a full standing position from a sitting position in 30 seconds. Score range from 0 and up with a higher score being considered as a better outcome.
Assessment of changes in Hand Grip Strength
Determination of potential changes in grip strength measured quantitatively using a hand dynamometer.
Assessment of changes in Balance
Determination of potential changes in balance using the Flamingo Balance Test. The participant stands on a 3 centimeter wide beam while holding the instructors hand. The tests then measures how many times the participant loses balance in 60 seconds.Score range from 0 and up with a lower score being considered as a better outcome.
Assessment of changes in Self-reported Physical Activity Behavior
Assesment of changes in self-reported physical activity behaviour using the Physical Activity Scale (PAS). The PAS measures self-reported amount of time spent on different physical activities, such as sports, work, and leisure time during 24 hours on an average weekday. The activities are organized in nine different metabolic equivalent (MET) levels ranging from sleep/rest (0.9 METs) to high-intensity physical activities (>6 METs). MET is the Metabolic Equivalent of Task and is a physiological measure expressing the energy cost of physical activities and is defined as the ratio of metabolic rate (and therefore the rate of energy consumption) during a specific physical activity to a reference metabolic rate. Therefore, higher MET scores in the Physical Activity Scale indicates a better outcome than lower scores.

Full Information

First Posted
January 4, 2018
Last Updated
September 13, 2018
Sponsor
Rigshospitalet, Denmark
Collaborators
University of Copenhagen, Mental Health Services in the Capital Region, Denmark
search

1. Study Identification

Unique Protocol Identification Number
NCT03409393
Brief Title
Feasibility and Relevance of High-Intensity Functional Training in Patients With First-Episode Psychosis
Acronym
COPUS
Official Title
Feasibility and Relevance of High-Intensity Functional Training in Patients Undergoing Specialised Early Intervention Treatment for First-Episode Psychosis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
January 22, 2018 (Actual)
Primary Completion Date
June 20, 2018 (Actual)
Study Completion Date
August 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark
Collaborators
University of Copenhagen, Mental Health Services in the Capital Region, Denmark

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed Description
The introduction of specialized early intervention (SEI) is stated to be the most successful recent addition to the treatment of schizophrenia and other psychotic illnesses. In Denmark, SEI teams called OPUS, offer early intervention treatment (i.e. OPUS treatment) to young patients between 18 and 35 years with first-episode psychosis. The OPUS treatment consists of three main pillars: modified assertive treatment, family involvement, and social skill training. OPUS treatment is delivered via multidisciplinary teams including psychiatrists, psychologists, nurses, social workers, physiotherapists, and vocational therapists. Despite considerable progress in treatment of schizophrenia, people diagnosed with schizophrenia live significantly shorter lives, compared to the rest of the population. The higher mortality rate can be partly explained by an increased risk of cardiovascular disease, including metabolic syndrome, which may be documented already in the first months after start of medical anti-psychotic treatment. It is widely acknowledged that physical activity constitutes a cornerstone in the prevention of cardiovascular disease and metabolic syndrome. Therefore, despite the influence of non-modifiable factors (e.g. genetics), it is reasonable to assume that physical activity can promote health and prevent somatic disease in people diagnosed with schizophrenia. However, currently, physical activity is not included in early intervention treatment of schizophrenia. Moreover, people with schizophrenia may experience anxiety, loss of motivation, apathy and social isolation, which can constitute significant barriers for adherence to physical activity. Existing knowledge in relation to physical activity behaviour change and adoption is therefore difficult to transfer directly to people with schizophrenia. Development and testing of new initiatives, which can be integrated into clinical practice, and offered complementary to SEI are thus warranted. Against this background, the aim of the current study (called the COPUS study) is to investigate, whether it is possible to recruit and retain young people with first-episode psychosis, to an 8-weeks supervised High-Intensity Functional Training (HIFT) intervention (i.e. COPUS intervention) and to investigate if oxygen uptake, body composition and physical function changes following participation in the COPUS intervention. The study is organized as a randomized mixed methods feasibility study. The COPUS intervention is offered in a private fitness centre in the local community. The intervention contains three training sessions of one hour duration per week, with the recommendation to the participants, to take part in at least two sessions per week. The investigators aim to include 30 participants whom will be randomly assigned (1:1) to either an intervention group receiving the COPUS intervention plus usual care (i.e. standard OPUS treatment) or a control group including only receiving usual care (i.e. standard OPUS treatment). Participants allocated to the control group are offered the COPUS intervention after eight weeks. The design and choice of methods reflect the complexity of the intervention (combination of social and physical elements that are difficult to control and isolate) and the desire to establish a scientifically informed basis for a subsequent, up-scaled, pragmatic randomized multicentre study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizotypal Disorder, First Episode Psychosis, Psychotic Disorders, Schizoaffective Disorder
Keywords
Human, Denmark, Adult, Adolescent, Young Adult, Male, Female, Physical Activity, Maximum Oxygen Consumption, Resistance Training, High-Intensity Functional Training, Aerobic Exercise, Motivation, Feasibility, Relevance, Health Behavior

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
The participants will be randomly assigned (1:1) to either an Intervention Group that in the initial study phase (week 0-8) receives the COPUS intervention plus usual care (i.e. OPUS treatment) or to a Control Group that only receives usual care in the initial phase. In the second phase of the study (week 8-16), participants allocated to the control group are offered the COPUS intervention.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
27 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
The COPUS intervention plus usual care (OPUS treatment).
Arm Title
Control Group
Arm Type
Other
Arm Description
Usual care (OPUS treatment).
Intervention Type
Other
Intervention Name(s)
The COPUS intervention
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Usual Care (OPUS treatment)
Intervention Description
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.
Primary Outcome Measure Information:
Title
Assessment of changes in Physical Fitness (VO2max)
Description
Assessed by the maximum amount of oxygen the body can utilize during a specified period of intense exercise.
Time Frame
Change from Baseline Physical Fitness (VO2max) at 2 months.
Title
Recruitment Rate
Description
Registration of patients enrolled in the study compared to the total number of eligible patients.
Time Frame
Registration of recruitment occurs in the 4 weeks prior to the baseline tests.
Title
Retention Rate
Description
Registration of the participants attendance in the High-Intensity Functional Training compared with the number of possible training sessions during the period.
Time Frame
From baseline up to 4 months.
Secondary Outcome Measure Information:
Title
Assessment of changes in body weight
Description
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining body weight.
Time Frame
Change from Baseline Body Weight at 2 months.
Title
Assessment of changes in fat percentage
Description
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining fat percentage.
Time Frame
Change from Baseline Fat Percentage at 2 months.
Title
Assessment of changes in bone mass
Description
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining bone mass.
Time Frame
Change from Baseline Bone Mass at 2 months.
Title
Assessment of changes in muscle mass
Description
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining muscle mass.
Time Frame
Change from Baseline Muscle Mass at 2 months.
Title
Assessment of changes in Visceral Fat
Description
The participants are placed on a bioelectric impedance scale which is a non-invasive valid measurement method for determining visceral fat.
Time Frame
Change from Baseline Visceral Fat at 2 months.
Title
Assessment of changes in Resting Blood Pressure
Description
The participants' Resting Blood Pressure are tested according to the American Heart Association practice guidelines for blood pressure Measurement.
Time Frame
Change form Baseline Resting Blood Pressure at 2 months.
Title
Assessment of changes in countermovement jump height
Description
Determination of potential changes in countermovement jump height measured using the non-invasive Optojump system (www.optojump.com)
Time Frame
Change form Baseline Jump Height at 2 months.
Title
Assessment of changes in Leg Muscle Strength
Description
Determination of potential changes in leg muscle strength by the non-invasive 30-Second Chair Stand test. The test measures how many times the participant can reach a full standing position from a sitting position in 30 seconds. Score range from 0 and up with a higher score being considered as a better outcome.
Time Frame
Change form Baseline Leg Muscle Strength at 2 months.
Title
Assessment of changes in Hand Grip Strength
Description
Determination of potential changes in grip strength measured quantitatively using a hand dynamometer.
Time Frame
Change form Baseline Hand Grip Strength at 2 months.
Title
Assessment of changes in Balance
Description
Determination of potential changes in balance using the Flamingo Balance Test. The participant stands on a 3 centimeter wide beam while holding the instructors hand. The tests then measures how many times the participant loses balance in 60 seconds.Score range from 0 and up with a lower score being considered as a better outcome.
Time Frame
Change form Baseline balance at 2 months.
Title
Assessment of changes in Self-reported Physical Activity Behavior
Description
Assesment of changes in self-reported physical activity behaviour using the Physical Activity Scale (PAS). The PAS measures self-reported amount of time spent on different physical activities, such as sports, work, and leisure time during 24 hours on an average weekday. The activities are organized in nine different metabolic equivalent (MET) levels ranging from sleep/rest (0.9 METs) to high-intensity physical activities (>6 METs). MET is the Metabolic Equivalent of Task and is a physiological measure expressing the energy cost of physical activities and is defined as the ratio of metabolic rate (and therefore the rate of energy consumption) during a specific physical activity to a reference metabolic rate. Therefore, higher MET scores in the Physical Activity Scale indicates a better outcome than lower scores.
Time Frame
Change from Baseline Physical Activity Behaviour at 2 months.
Other Pre-specified Outcome Measures:
Title
Monitoring of training intensity (for the Intervention Group only)
Description
Determination of whether the training intensity is adequate to increase Physical Fitness, the workload during training is continuously measured. A validated device called Actiheart which is both an accelerometer and a heart rate monitor is used to measure workload.
Time Frame
Through study completion, an average of 4 months
Title
Adverse events
Description
We will continuously record adverse events that may arise as a result of the intervention, including physical damage, discomfort and any deterioration of symptoms. The adverse events will be registred both in the intervention period and in the Control Group training period.
Time Frame
Through study completion, an average of 4 months
Title
Resource Consumption
Description
In order to evaluate the sustainability of the intervention, we want to register how much time (in minutes) OPUS staff spends on the project
Time Frame
Through study completion, an average of 4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18 and 35 years Diagnosed with Schizophrenia or Schizotypal disorders Undergoing OPUS treatment for at least 6 months or stabilized medical anti-psychotic treatment Danish speaking Exclusion Criteria: Physical contraindications for physical activity Pregnant (self-reported) Unable to give adequately informed consent Mentally disabled
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julie Midtgaard, Ph.D.
Organizational Affiliation
The University Hospitals Centre for Health Research (UCSF) / Copenhagen University Hospital (Rigshospitalet)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Helle Schnor, Ph.D.
Organizational Affiliation
Mental health services in the Capital Region of Denmark, Psychiatric Center Glostrup
Official's Role
Study Director
Facility Information:
Facility Name
OPUS
City
Brøndby
ZIP/Postal Code
2605
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
34412705
Citation
Midtgaard J, Schnor H, Bjerre ED, Jespersen T, Jelsoe N, Frolund N, Seier S, Ronbog JW, Nordsborg NB, Ebdrup BH. Exercise training complementary to specialised early intervention in patients with first-episode psychosis: a feasibility randomised trial. Pilot Feasibility Stud. 2021 Aug 19;7(1):162. doi: 10.1186/s40814-021-00900-5.
Results Reference
derived
PubMed Identifier
31226959
Citation
Larsen LQ, Schnor H, Tersbol BP, Ebdrup BH, Nordsborg NB, Midtgaard J. The impact of exercise training complementary to early intervention in patients with first-episode psychosis: a qualitative sub-study from a randomized controlled feasibility trial. BMC Psychiatry. 2019 Jun 21;19(1):192. doi: 10.1186/s12888-019-2179-3.
Results Reference
derived
Links:
URL
http://www.ucsf.dk
Description
Official institutional website

Learn more about this trial

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

We'll reach out to this number within 24 hrs