Influence of the Pilates method on the health of older adults
| ISRCTN | ISRCTN39798808 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN39798808 |
| Sponsor | University of Coimbra |
| Funder | Universidade de Coimbra |
- Submission date
- 12/09/2026
- Registration date
- 26/09/2026
- Last edited
- 21/09/2026
- Recruitment status
- No longer recruiting
- Overall study status
- Ongoing
- Condition category
- Other
Plain English summary of protocol
Background and study aims
Pilates is a form of exercise that may help older adults maintain or improve their physical and overall health. However, more research is needed to understand its effects on functional capacity, physical fitness, quality of life, and metabolic and cellular health in older adults.
This study aims to investigate whether a 12-week Pilates exercise programme can improve functional capacity, physical health, quality of life and well-being, and clinical, metabolic and cellular health in older adults. The study will also examine whether different levels of physical activity are associated with different responses to Pilates.
Who can participate?
The study will include adults aged 60 years and older who meet the study eligibility criteria. Participants must be able to understand the study procedures, provide informed consent, and safely perform the physical assessments and exercise programme.
What does the study involve?
Approximately 60 participants will take part in the study. Participants will be divided into three groups: a sedentary control group, a sedentary group that will participate in Pilates, and a physically active group that will participate in Pilates.
Participants in the Pilates groups will take part in supervised Pilates sessions twice a week for 12 weeks. Each session will last approximately 45–50 minutes and will include exercises adapted to older adults.
All participants will undergo assessments before and after the study period. These assessments will include measures of physical function and fitness, balance, muscle strength, flexibility, body composition, cardiovascular and metabolic health, quality of life and well-being. Biological samples will also be collected to assess metabolic, inflammatory and cellular markers.
The sedentary control group will not participate in the Pilates programme but will complete the study assessments.
What are the possible benefits and risks of participating?
Participants may benefit from taking part in a structured exercise programme and from increased awareness of aspects of their physical and health status. However, individual health improvements cannot be guaranteed.
The Pilates programme and physical assessments may cause temporary muscle soreness, tiredness or discomfort. There may also be a small risk of loss of balance or injury during physical assessments or exercise. Appropriate safety procedures will be followed, and participants will be monitored throughout the assessments and exercise sessions.
Blood sample collection may cause temporary discomfort, bruising or, rarely, dizziness or fainting.
Where is the study run from?
The study is being conducted by the Faculty of Sport Sciences and Physical Education, University of Coimbra, Portugal.
When is the study starting and how long is it expected to run for?
The intervention is expected to start in September 2026 and will last 12 weeks. Participant assessments and data collection will take place before and after the intervention period. The overall study is expected to continue beyond the intervention period to allow for completion of data analysis and reporting.
Who is funding the study?
The study is being conducted as part of a doctoral research project at the University of Coimbra. The study is supported by the Faculty of Sport Sciences and Physical Education, University of Coimbra. No commercial funding is involved.
Who is the main contact?
Daniel Neto Custódio
Faculty of Sport Sciences and Physical Education
University of Coimbra, Portugal
daniel.neto.custodio@gmail.com
Contact information
Principal investigator, Scientific, Public
Rua Vitorino Nemésio, Nº1, R/C, Direito, Fração B
Coimbra
3030-361
Portugal
| 0009-0008-1039-6383 | |
| Phone | +351 919771221 |
| daniel.neto.custodio@gmail.com; uc2007020840@student.uc.pt |
Study information
| Primary study design | Interventional |
|---|---|
| Allocation | Randomized controlled trial |
| Masking | Blinded (masking used) |
| Control | Active |
| Assignment | Parallel |
| Purpose | Prevention |
| Scientific title | Effects of a 12-week Pilates intervention on physical fitness, body composition, blood biomarkers, and functional health in older adults compared with sedentary and physically active older adults not participating in Pilates |
| Study objectives | This study aims to collect, analyse, and generate scientific evidence to address the following research questions: 1. Does Pilates practice positively influence functional capacity and quality of life in older adults? 2. Which conditions of Pilates practice tend to produce the most significant outcomes? 3. What is the impact of Pilates practice on cardiovascular risk factors and physical fitness variables, including strength, endurance, and flexibility, in older adults? 4. What is the impact of the Pilates method on metabolic and cellular health in older adults? |
| Ethics approval(s) |
Submitted 24/05/2026, University of Coimbra Ethics Committee (University of Coimbra, Paço das Escolas, Portugal Universidade de Coimbra, Coimbra, 3004-531 Coimbra, Portugal; +351 239 859 900; comissaoetica_research@uc.pt), ref: CE/FCDEF-UC/00132026 |
| Health condition(s) or problem(s) studied | Effects of Pilates exercise on health and healthy ageing in older adults |
| Intervention | Participants will undergo baseline assessments before being allocated to one of three study groups: (1) a sedentary control group, which will not receive the Pilates intervention and will undergo the study assessments only; (2) a sedentary Pilates group, which will participate in a supervised Pilates exercise programme; and (3) an active Pilates group, consisting of physically active older adults who will also participate in the Pilates exercise programme. Participants in the Pilates groups will undertake supervised Pilates sessions twice per week, with each session lasting approximately 45 minutes, for 12 weeks. The Pilates programme will be delivered by qualified instructors with 10 or more years of experiance and will consist of structured mat-based Pilates exercises appropriate for older adults. Participants in all groups will undergo the same baseline and post-intervention assessments. These assessments will include measures of functional capacity, physical fitness, anthropometry and body composition, cardiovascular risk factors, metabolic health, cellular and inflammatory markers, and quality of life. Assessments will include physical performance tests, questionnaires, body composition analysis, cardiovascular measurements, and biological sample collection, as specified in the study protocol. The study employs a partially randomised allocation procedure. Allocation is initially determined according to predefined participant characteristics, particularly baseline physical activity status, as these characteristics are integral to the study design and determine eligibility for specific study groups. Consequently, not all participants are eligible for allocation to all study groups. Among participants who are eligible for allocation between the relevant intervention and control groups, group allocation is subsequently performed using an online randomisation tool. This approach allows the study to maintain the predefined group structure while ensuring an objective and reproducible allocation procedure wherever random allocation is applicable. |
| Intervention type | Behavioural |
| Primary outcome measure(s) |
|
| Key secondary outcome measure(s) | |
| Completion date | 15/12/2026 |
Eligibility
| Participant type(s) | |
|---|---|
| Age group | Mixed |
| Lower age limit | 60 Years |
| Upper age limit | 90 Years |
| Sex | All |
| Target sample size at registration | 74 |
| Key inclusion criteria | 1. Adults aged 60 years or older 2. Able to understand the study procedures and provide written informed consent 3. Able to walk independently, with or without usual walking aids 4. Able to participate safely in the Pilates exercise programme and physical assessments, as determined by the study team 5. Willing and able to attend the scheduled study assessments and intervention sessions, where applicable 6. For participants allocated to the Pilates groups, no participation in a regular Pilates programme during the previous 6 months |
| Key exclusion criteria | 1. Presence of a medical condition or physical limitation that contraindicates participation in moderate-intensity physical exercise or Pilates, as determined by the study team 2. Inability to walk independently or to safely perform the physical assessments required by the study 3. Cognitive or communication impairment that prevents understanding the study procedures or providing informed consent 4. Current participation in a regular Pilates exercise programme, for participants allocated to groups for which previous Pilates participation is an exclusion criterion 5. Planned absence or inability to attend the required study assessments or intervention sessions 6. Any other condition identified by the research team that would prevent safe participation or compromise the validity of the study assessments |
| Date of first enrolment | 10/09/2026 |
| Date of final enrolment | 16/09/2026 |
Locations
Countries of recruitment
- Portugal
Study participating centres
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|
Editorial Notes
21/09/2026: Trial's existence confirmed by University of Coimbra Ethics Committee.