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Moderate-to-Vigorous Intensity Physical Activity and Severe Mental Illness (+MoviMENT)

U

University of Vic - Central University of Catalonia

Status

Active, not recruiting

Conditions

Mental Health Issue

Treatments

Behavioral: Moderate-to-vigorous intensity physical activity program (+moviMENT)

Study type

Interventional

Funder types

Other

Identifiers

NCT06338917
File 2022 DI 61

Details and patient eligibility

About

Twenty-five percent of the population worldwide will experience a severe mental illness during their lifetime (World Health Organization, 2017). These people present strong barriers to adhering to moderate and vigorous-intensity continuous training. It is fundamental to overcome these barriers for practicing moderate-to-vigorous physical activity by adding behavioural change techniques into physical activity interventions (Maurus et al., 2023), in order to design and implement sustainable interventions that empower people to engage in it.

The overall aims will be to evaluate the efficacy of +moviMENT, a 28-week intervention program, designed to increase MVPA time in patients with SMI, and to assess the effects of the program on a range of indicators, in comparison with a 'usual care' control group.

Full description

This is a pragmatic controlled clinical trial with intervention and control group, in which patients will be recruited from two different services from different cities. Patients who will meet the inclusion criteria (>16 years, severe mental illness diagnosis, not medical risk to practice MVPA, living in the community) from one service will be assigned to the intervention and those from the other to the control group. The intervention comprises 16 weeks of group based High Intensity Interval Training (HIIT), with transition to individual community based Vigorous Intermittent Lifestyle Physical Activity (VILPA) over the next 12 weeks - for a total intervention period of 28 weeks. Primary outcomes measures (clinical and functional) and secondary (personal recovery, self-perception and device-measured fitness, physical activity and sedentary behaviour and experience) will be assessed at baseline and after 16, 28 and 40 weeks, after follow-up. Group differences in change scores will be assessed using linear mixed-effects models with time, group, and their interaction as fixed effects, accounting for within-subject correlations.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 69 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

  • Outpatients (non-hospitalised) registered in one of two mental health services.
  • SMI diagnosis, according to the 5th edition of the 5th Diagnostic and Statistical Manual of mental disorders (DSM-5) [52].
  • Living in the community
  • Not having any contraindications or medical risk to MVPA.
  • Age 18 to 69 years.
  • Willing and able to provide informed consent.

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 2 patient groups

Intervention group
Experimental group
Description:
Participation in a moderate-to-vigorous intensity physical activity program a part from the usual health care treatment
Treatment:
Behavioral: Moderate-to-vigorous intensity physical activity program (+moviMENT)
Control group
No Intervention group
Description:
Following the usual health care treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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