Telehealth-Based vs In-Person Aerobic Exercise in Individuals With Schizophrenia: Comparative Analysis of Feasibility, Safety, and Efficacy.

Publication date: Feb 14, 2025

Aerobic exercise (AE) training has been shown to enhance aerobic fitness in people with schizophrenia. Traditionally, such training has been administered in person at gyms or other communal exercise spaces. However, following the advent of the COVID-19 pandemic, many clinics transitioned their services to telehealth-based delivery. Yet, at present, there is scarce information about the feasibility, safety, and efficacy of telehealth-based AE in this population. To examine the feasibility, safety, and efficacy of trainer-led, at-home, telehealth-based AE in individuals with schizophrenia. We analyzed data from the AE arm (n=37) of a single-blind, randomized clinical trial examining the impact of a 12-week AE intervention in people with schizophrenia. Following the onset of the COVID-19 pandemic, the AE trial intervention transitioned from in-person to at-home, telehealth-based delivery of AE, with the training frequency and duration remaining identical. We compared the feasibility, safety, and efficacy of the delivery of trainer-led AE training among participants undergoing in-person (pre-COVID-19; n=23) versus at-home telehealth AE (post-COVID-19; n=14). The telehealth and in-person participants attended a similar number of exercise sessions across the 12-week interventions (26. 8, SD 10. 2 vs 26. 1, SD 9. 7, respectively; P=. 84) and had similar number of weeks with at least 1 exercise session (10. 4, SD 3. 4 vs 10. 6, SD 3. 1, respectively; P=. 79). The telehealth-based AE was associated with a significantly lower drop-out rate (telehealth: 0/14, 0%; in-person: 7/23, 30. 4%; P=. 04). There were no significant group differences in total time spent exercising (telehealth: 1246, SD 686 min; in-person: 1494, SD 580 min; P=. 28); however, over the 12-week intervention, the telehealth group had a significantly lower proportion of session-time exercising at or above target intensity (telehealth: 33. 3%, SD 21. 4%; in-person: 63. 5%, SD 16. 3%; P. 99) or in the percentage of weeks per participant with at least 1 exercise-related adverse event (telehealth: 31%, SD 33%; in-person: 40%, SD 33%; P=. 44). There were no significant differences between the telehealth versus in-person groups regarding changes in aerobic fitness as indexed by maximum oxygen consumption (VO2max; P=. 27). Our findings provide preliminary support for the delivery of telehealth-based AE for individuals with schizophrenia. Our results indicate that in-home telehealth-based AE is feasible and safe in this population, although when available, in-person AE appears preferable given the opportunity for social interactions and the higher intensity of exercises. We discuss the findings’ clinical implications, specifically within the context of the COVID-19 pandemic, as well as review potential challenges for the implementation of telehealth-based AE among people with schizophrenia.

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Concepts Keywords
Gyms Adult
Schizophrenia aerobic fitness
Vo2max clinical trial
Week COVID-19
COVID-19
Exercise
exercise
Exercise Therapy
Feasibility Studies
Female
Humans
Male
maximum oxygen consumption
Middle Aged
psychosis
safety
Schizophrenia
schizophrenia
Single-Blind Method
telehealth
Telemedicine
telemedicine
Treatment Outcome
VOmax

Semantics

Type Source Name
disease MESH Schizophrenia
disease MESH COVID-19 pandemic
disease IDO intervention
drug DRUGBANK Oxygen
drug DRUGBANK Methylphenidate
disease MESH Mental Illness
drug DRUGBANK Trestolone
disease MESH psychosis
disease MESH Sedentary lifestyle
disease MESH symptom burden
disease MESH depression
disease IDO site
drug DRUGBANK Ethanol
disease MESH substance abuse
drug DRUGBANK Nicotine
disease IDO history
disease MESH seizures
disease MESH sequelae
disease MESH abnormalities
disease MESH hypothyroidism
disease MESH Syndrome
disease MESH Blisters
disease MESH Dyspnea
disease MESH Joint pain
disease IDO blood
disease MESH emergency
disease MESH metabolic syndrome
disease MESH bipolar disorder
disease MESH major depressive disorder
drug DRUGBANK Icosapent
drug DRUGBANK Minaprine
pathway REACTOME Reproduction

Original Article

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