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Impact of Multicomponent and Stability Training on Fitness and Function in Active Older Women

Effect of Multicomponent Training and Stability Exercises on Body Composition, Physical Fitness, and Functional Movement Capability in Active Older Women: A Non-Randomized Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07204886
Acronym
STABLE-WOMEN
Enrollment
40
Registered
2025-10-02
Start date
2025-08-21
Completion date
2026-01-12
Last updated
2026-02-17

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

Conditions

Body Composition, Functional Capacities, Physical Fitness

Keywords

Functional movement screening, Performance, Physical Activity, Older adults

Brief summary

Purpose of the Study The purpose of this study is to examine the effects of a multicomponent training program combined with stability exercises on body composition, physical fitness, and functional movement capabilities in active older women. It aims to determine whether these combined exercises can improve physical health and movement quality in this population. Research Question What are the effects of multicomponent training and stability exercises on body composition, physical fitness, and functional movement capability in active older women?

Detailed description

Study Title Effect of Multicomponent Training and Stability Exercises on Body Composition, Physical Fitness, and Functional Movement Capability in Active Older Women: A Non-Randomized Study This study will investigate the effects of a 14-week multicomponent training program combined with stability exercises on body composition, physical fitness, and functional movement capability in active older women. Participants will be assigned to either an intervention group undergoing the exercise protocol or a control group maintaining their usual activities. Pre- and post-intervention assessments will be conducted to evaluate the outcomes. Study Type Design: Interventional (Non-Randomized), Controlled Trial Allocation: Non-randomized Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Prevention Time Perspective: Prospective Duration: 14 weeks

Interventions

OTHERMulticomponent training and stability exercise

The training program will span 14 weeks. Participants will engage in structured sessions twice a week (on Tuesdays and Thursdays), with each session lasting 60 minutes. The sessions will consist of aerobic, balance, Dynamic Neuromuscular Stabilization (DNS) and stability exercises, strength exercises (using body weight and the Swedish bar), and flexibility exercises. Each training session will begin with a warm-up phase, including five minutes of dynamic stretching to prepare the body for the physical demands of the session. Following the warm-up, participants will perform 15 minutes of low-impact aerobic exercises, such as marching, knee lifts, leg curls, lunges, and kicks, incorporating coordinated arm movements. Next, participants will complete 15 minutes of balance, DNS, and stability exercises. This will be followed by 20 minutes of strength training exercises. Each session will conclude with a 5-minute cooldown and flexibility segment to promote

Sponsors

University of Novi Sad
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

* Study type: Non-randomized, controlled trial, pre- and post-test design * Groups: Intervention group (IG, n =15) underwent a structured 14-week training protocol Control group (CG, n=15) continued their regular daily activities without participating in any organized training program \- Treatment duration: 14 weeks

Eligibility

Sex/Gender
FEMALE
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. were women older than 65 years and did not live in nursing homes or community living 2. physically independent individuals able to perform daily living tasks 3. not present absence of physical limitations that might limit their engagement in exercise 4. absence of cardio metabolic and neuromuscular disease that could negatively affect exercise performance

Exclusion criteria

1. fracture of extremities in the last 3 months 2. functional limitation (motor, auditory, and visual disorders) 3. dropout and absence of participants at any measurement, and absence in more than 25% of the training sessions

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in the the 30-second Chair Stand test (30-s CST)14 weeksThe 30-second Chair Stand test (30-s CST) will be used to evaluate lower body strength, with test procedures and reliability based on Rikli and Jones (2013).

Secondary

MeasureTime frameDescription
Change from Baseline in Functional Movement Capability14 weeksThe test will be conducted using a standardized Functional Movement Screen (FMS) to assess functional movement capability
Change from Baseline in Body Composition14 weeksThe body composition were assessed using bioelectrical impendence

Countries

Serbia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026