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How can a jump training program in Pilates benefit elderly people?

Analysis of the Jump Exercise on the Pilates Reformer Apparatus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9rhyqy4
Enrollment
80
Registered
2026-03-26
Start date
2024-07-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Physical Functional Performance Aging

Interventions

This is a randomized clinical trial with two parallel groups, composed of 80 older adults randomly allocated into a control group (n=40) and an experimental group (n=40). Participants exercised two ti
lower limb strengthening exercises such as footwork (10 repetitions in five standard positions), bilateral and unilateral bridges (10 repetitions each), leg circles (10 repetitions in each direction),
and upper limb exercises including pushing and pulling actions (3 sets of 10 repetitions) and scapular stability drills with elastic bands (3 sets of 10 repetitions). The session ended with breathing

Sponsors

Universidade do Estado de Santa Catarina
Lead Sponsor
Universidade do Estado de Santa Catarina
Collaborator

Eligibility

Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Adults aged 60 years or older; Both sexes; Previous participation in Pilates classes for at least six months with a frequency of two or more sessions per week; availability to attend the 12 intervention sessions during the study period; signed informed consent form

Exclusion criteria

Exclusion criteria: Severe cognitive impairment; cardiovascular or respiratory disorders; hypertension; history of musculoskeletal or joint injuries and/or bone fractures in the lower limbs in the last 6 months

Design outcomes

Primary

MeasureTime frame
Expected outcome 1: To evaluate the feasibility of integrating high-velocity jump training into Pilates Reformer sessions for older adults, assessed through adherence rate, acceptability of the intervention, and occurrence of adverse events during the 6-week intervention period. Adherence will be verified by calculating the percentage of attended sessions relative to the total number of prescribed sessions. Acceptability will be verified using a structured questionnaire administered at the end of the intervention. Safety will be verified through systematic recording of adverse events throughout the intervention period. The protocol will be considered feasible if adherence is = 75%, no serious adverse events occur, and the majority of participants report positive acceptability.;Expected outcome 2: To evaluate changes in lower limb functional performance after the 6-week intervention, assessed using the Five Times Sit-to-Stand test and the Timed Up and Go test. Performance will be verified by the time (in seconds) required to complete each test. Pre- and post-intervention values will be compared to observe potential functional changes. ;Expected outcome 3: To evaluate changes in jump performance after the 6-week intervention through peak velocity, measured during the jump task on the Pilates Reformer and expressed in meters per second (m/s). Pre- and post-intervention values will be compared to observe possible changes in performance.;Found outcome 1:After the 6-week intervention, participants showed high acceptability of the exercise program. Responses indicated a high willingness to participate in similar exercise programs in the future. No relevant differences were observed between groups over time for individual acceptability items or for the total acceptability score. Adherence and dropout rates were also similar between groups.;Found outcome 2: After the 6-week intervention, significant improvements were observed in the 5STS test in the Pilates + Jump group, in

Secondary

MeasureTime frame
No secondary outcomes are expected

Countries

BR

Contacts

Public ContactJader Beck

Universidade do Estado de Santa Catarina

jaderbeck@hotmail.com+55(48)996321284

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Apr 4, 2026