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Gymnastics and Multicomponent Training Intervention in Community-dwelling Older Adults

11 augustus 2026 bijgewerkt door: Marcos Luciano Pimenta Pinheiro, Federal University of the Valleys of Jequitinhonha and Mucuri

Community-based Multicomponent Training and Gymnastics Intervention

Introduction: Extension projects focused on physical activity can offer health practices and promote quality of life for participants of different ages. Investing in extension projects with a research interface can contribute to relevant insights for teaching knowledge. Furthermore, the progressive aging of the population makes it essential to identify individuals at risk of functional decline and to implement evidence-based interventions that allow for the reduction of these losses, enabling a better quality of life for the elderly. The WHO developed the guideline that addresses healthy development, with strategies to promote healthy aging based on solid concepts, with data on their applicability in a real-life scenario, especially from intervention studies. Objective: To evaluate the impact of interventions focused on Gymnastics and multicomponent training on the intrinsic capacity of adult and elderly participants in extension projects at UFBA. Methodology: This is an intervention study within an extension project with a research focus, encompassing adult individuals (participants in MOVEGINBA) and elderly individuals of both sexes, aged 60 years or older (participants in the MOVEGINBA 60+ project). Participants will be evaluated regarding anthropometric, sociodemographic characteristics, health conditions, and physical-functional performance. As well as quality of life, sleep quality, fear of falling, and independence in activities of daily living. Tests and interviews will be conducted before and after the intervention. The results of this study will be fundamental to understanding the implications of the multicomponent gymnastics/training intervention for the participants.

Keywords: Aging; Physical capacity; Gymnastics.

Studie Overzicht

Gedetailleerde beschrijving

University outreach programs should be offered to promote the health and quality of life of the general population, taking into account diverse target audiences. Viewing outreach as an extension of the university into the community, the MOVEGINBA project-registered with PROEXC under number 23132-has been conducted in the Faculty of Education's exercise studio since the first semester of 2025, serving adults, students from various academic programs, and the general public through training activities. Concurrently, the global population is aging rapidly, with significant impacts on economies and healthcare systems. In Brazil, the population aged 65 and older is projected to rise from the current 20 million in 2020 (9.8% of the population) to over 50 million by 2050 (21.8% of the population). Given this scenario, public policies capable of mitigating age-related loss of functional capacity are both urgent and essential. In its report on health and aging, the WHO defined healthy aging as a process requiring the promotion and maintenance of functional capacities that enable individual well-being. Thus, optimizing the health of older adults through strategies that identify high-risk individuals and propose actions to prevent or delay the progression of functional decline appears to be the best approach to reducing the strain on healthcare systems.

In 2017, the WHO published guidelines for healthy development, which address health and well-being and encompass physical activity for individuals. With this perspective in mind, extension activities are encouraged and take place within the university setting, focusing on older adults; to this end, we offer the MOVEGINBA 60+ program-registered with PROEXC under number 23351-which addresses the specific gaps and needs of this demographic. Consequently, gymnastics-based extension projects are conducted at the Federal University of Bahia.

It is essential to understand the implications of such projects for participants regarding emotional health, physical capacity, agility, social interaction, and the intrinsic capacity of older adults. Therefore, this study aims to understand the implications of gymnastics-focused interventions for participants and to analyze their impact on the target population. This initiative is an extension project with a research component-encompassing undergraduate capstone projects and graduate studies-that contributes significantly to people's quality of life.

Conditions: Must be an older adult (over 60 years of age). Must be capable of performing any physical activity independently. Participants may have hypertension, diabetes, or multiple comorbidities, provided they fall within the 1 to 7 range on the Clinical Frailty Scale (ranging from robust to mildly frail).

Studietype

Ingrijpend

Inschrijving (Geschat)

80

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Estado de Bahia
      • Salvador, Estado de Bahia, Brazilië, 40170115
        • Faculdade de Educação

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Ja

Beschrijving

Inclusion criteria: Community-dwelling older adults (60 years of age or older), and able to travel to the training center.

Exclusion criteria: Score 7, 8 or 9 on the Clinical Frailty Scale and those with any impediment to performing physical exercise.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Preventie
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Multicomponent training intervention
Multicomponent training intervention - Protocol includes mobility, resistance exercises for the lower and upper limbs and major muscle groups, and aerobic exercises. The intervention will take place twice a week for one hour, following a 12-week protocol.

The interventions will take place twice a week, on two days (Mondays and Wednesdays) with two groups lasting one hour each. The exercises will include joint mobility training, followed by strength training with body weight and the use of elastic bands, dumbbells, sticks, and the like. Subsequently, there will be an aerobic part, lasting 30 minutes, in which the heart rate will be increased, with the use of sound and rhythms. Following this, there will be a cool-down, with a reduction in activities.

Participants will be evaluated before and after the intervention, after 12 weeks, with variables that include intrinsic capacity such as mobility, psychological state, vitality, sensory and cognitive domain.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Intrinsic capacity
Tijdsspanne: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Cognition: Montreal Cognitive Assessment - MOCA
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity
Tijdsspanne: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Mobility: 5-times sit-to-stand test and 6-minutr walk test
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity
Tijdsspanne: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Psychological:15 itens - Geriatric Depression Scale -GDS-15
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity
Tijdsspanne: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Vitality: Handgrip strength
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity:
Tijdsspanne: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Hearing: Self-reported - Self-reported - Participants are asked if they have any hearing problems.
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity
Tijdsspanne: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Vision: self-reported - Participants are asked if they have any vision problems, if they have difficulty seeing up close or far away, if they have any eye disease, or if they are undergoing medical treatment for diabetes or hypertension.
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Anthropometry
Tijdsspanne: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
BMI: Weight and height will be used to calculate Body Mass Index.
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Nuttige links

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

20 februari 2026

Primaire voltooiing (Geschat)

20 december 2027

Studie voltooiing (Geschat)

20 december 2028

Studieregistratiedata

Eerst ingediend

26 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

11 augustus 2026

Eerst geplaatst (Werkelijk)

17 augustus 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

17 augustus 2026

Laatste update ingediend die voldeed aan QC-criteria

11 augustus 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Due to participant confidentiality, the data may be shared, but participant identification will not be disclosed.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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