NCT07204886

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?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 21, 2025

Completed
22 days until next milestone

First Submitted

Initial submission to the registry

September 12, 2025

Completed
20 days until next milestone

First Posted

Study publicly available on registry

October 2, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 12, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 12, 2026

Completed
Last Updated

February 17, 2026

Status Verified

September 1, 2025

Enrollment Period

5 months

First QC Date

September 12, 2025

Last Update Submit

February 12, 2026

Conditions

Keywords

Functional movement screeningPerformancePhysical ActivityOlder adults

Outcome Measures

Primary Outcomes (1)

  • Change from Baseline in the the 30-second Chair Stand test (30-s CST)

    The 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).

    14 weeks

Secondary Outcomes (2)

  • Change from Baseline in Functional Movement Capability

    14 weeks

  • Change from Baseline in Body Composition

    14 weeks

Study Arms (2)

Intervention group underwent a structured 14-week training protocol

EXPERIMENTAL

Intervention group (IG, n =15) underwent a structured 14-week training protocol

Other: Multicomponent training and stability exercise

Control group continued their regular daily activities without participating in any organ

NO INTERVENTION

Control group (CG, n=15) continued their regular daily activities without participating in any organized training program

Interventions

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

Intervention group underwent a structured 14-week training protocol

Eligibility Criteria

Age65 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsThis study focuses exclusively on women aged 65 years and older because this age group is at higher risk for age-related declines in physical fitness, muscle mass, balance, and functional mobility. Older women, in particular, experience greater rates of sarcopenia, osteoporosis, and functional limitations compared to men, which can increase their risk of falls and loss of independence. By targeting this population, the study aims to address the specific needs and challenges faced by older women, providing more relevant and applicable results to improve their health and quality of life. Additionally, including a homogeneous age and sex group helps reduce variability and allows for clearer interpretation of the intervention's effects.
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Sport and Physical Education

Novi Sad, 21000, Serbia

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: * 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
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 12, 2025

First Posted

October 2, 2025

Study Start

August 21, 2025

Primary Completion

January 12, 2026

Study Completion

January 12, 2026

Last Updated

February 17, 2026

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations