ClinicalTrials.Veeva

Menu

Physical Exercise in Patients With First Psychotic Episode

U

University of Salamanca

Status

Not yet enrolling

Conditions

Telomere Length
First Episode Psychosis (FEP)
Exercise

Treatments

Other: Other: Strength physical exercise programme
Other: Other: Normal life

Study type

Interventional

Funder types

Other

Identifiers

NCT07207538
ExerciseFirstPsychoticEpisode

Details and patient eligibility

About

Justification: Patients with first-episode psychosis are at increased risk of premature ageing and early mortality, associated with telomere shortening and increased inflammatory markers. Physical exercise has shown protective effects in the general population, but there are no intervention studies in this population.

Objective: To evaluate the effect of a strength training programme on telomere length and other markers of cellular ageing in people with a first episode of psychosis.

Material and methods: Quasi-experimental study with patients aged 18-35 years included in the PRINT programme (Salamanca). Standard treatment will be compared with standard treatment plus a 12-week strength training programme. Telomere length (qPCR), inflammatory and senescence markers (proteomics), body composition, frailty and quality of life will be analysed.

Applicability: The results could support the inclusion of physical exercise programmes as a complementary intervention in early psychosis care, promoting overall health, quality of life and reducing the gap in life expectancy compared to the general population.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • be at least 18 years of age
  • Having experienced a first psychotic episode in the last 3 years

Exclusion criteria

  • are unable to read and understand the patient information sheet and sign the informed consent form.

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Experimental: Intervention group
Experimental group
Description:
n additional strength training programme will be carried out for 12 weeks with 2 sessions per week. The sessions will last approximately 50 minutes and will be divided into 3 distinct parts: The first part will consist of a warm-up with a part of aerobic exercise that will last approximately 15 minutes. This will be followed by the main part of strength training with a circuit of 6 exercises (3 series x 12 repetitions) which will last approximately 25 minutes. Finally, there will be a cool down phase with breathing exercises to allow people to recover.
Treatment:
Other: Other: Strength physical exercise programme
Sham Comparator: Control group
Sham Comparator group
Description:
Subjects in the control group will continue with their normal life and carry out all the activities they have been doing previously.
Treatment:
Other: Other: Normal life

Trial contacts and locations

0

Loading...

Central trial contact

Juan Luis Sánchez González Phd

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems