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The MOVEMENT study: Exercise and quality of life in people with mental illness

The MOVEMENT study: Exercise and quality of life in people with mental illness

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624001148561
Acronym
MOVEMENT
Enrollment
196
Registered
2024-09-23
Start date
2025-04-15
Completion date
2026-07-14
Last updated
2026-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This study seeks to assess the influences on recovery-oriented quality of life (ReQoL) in adults (i.e., over 16 years) who are receiving treatment for a severe mental illness (SMI). The aim of this study is to evaluate the effectiveness of an AEP service implemented within routine mental health care settings. Participants will be asked to complete questionnaire and physiological assessments at three time-points separated by three months (baseline, 3-months, 6-months). Participants will also be given the option of participating in an exercise service delivered by an Accredited Exercise Physiologist (AEP), involving at least one group-based exercise session each week.

Interventions

This is an effectiveness-implementation Hybrid Type 1 design designed to evaluate the clinical-effectiveness of participation in an exercise service delivered by an Accredited Exercise Physiologist (AEP) for improving the quality of life in individuals with severe mental illness (SMI). This design will be a quasi-experimental trial, in which participant consent to complete the research measures and have the option of accessing an AEP service as part of their participation in the study. Analyses

This is an effectiveness-implementation Hybrid Type 1 design designed to evaluate the clinical-effectiveness of participation in an exercise service delivered by an Accredited Exercise Physiologist (AEP) for improving the quality of life in individuals with severe mental illness (SMI). This design will be a quasi-experimental trial, in which participant consent to complete the research measures and have the option of accessing an AEP service as part of their participation in the study. Analyses will compare participants who accept vs decline the AEP service. The study will take place in five mental health service sites in Queensland, specifically in the Brisbane areas. The partner organisations involved are Hospital Health Services (HHSs: Metro North Hospital and Health Service) and non-government organisations (NGOs: Communify QLD; Neami National; Stride; Richmond Fellowship QLD). The primary aims of the study is to evaluate the effectiveness of the AEP service for improving QoL in people with SMI. Consenting participants self-allocate into either the control or intervention group. The intervention group will receive an integrated exercise service delivered and supervised by an AEP. The exercise intervention will consist of at least one 60 min session per week. Exercise programs will be individualised to participants and conducted as one-on-one or group sessions in various settings, such as community gyms and outdoor environments. Adherence to the intervention will be monitored using a participant / attendance checklist. Participants will have access to the AEP service for 6 months. Exercise sessions will be offered weekly over this intervention period, in 8-10-week blocks. Assessments are completed at three time-points (baseline, 3-month and 6-month follow-up). Exercise intensity will be monitored using a Borg rating of perceived exertion (i.e., 1-10) scale. Session intensity will be modified based on participant requirements. The AEP will engage participants in individual goal setting focused on completing exercises outside supervised sessions. Individual goal setting and exercise prescriptions will be tailored to individual preferences and abilities and include a variety of aerobic (i.e., outdoor walking and running, and machine based activities such as treadmill, rowing, ski, and bike intervals), and resistance exercises (i.e., body weight, free weight, and barbell/machine exercises, including push-ups, squats, dead-lifts, shoulder press, bench press, inverted and bent-over rows, leg curls and leg extensions) and physically active recreation (e.g., sports, active groups), to maximise participant’s ability to participate, safely, in the program.

Sponsors

Griffith University
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Receiving mental health treatment from public services or NGOs Age: 18 years of age and over Diagnosis of severe mental illness (ICD-10 codes F20-F33, F60&61)

Exclusion criteria

Impaired capacity to consent <18 years of age

Outcome results

None listed

Source: ANZCTR · Data processed: Aug 31, 2026