Four-Week Multicomponent Exercise Program in Older Adults
Effects of a 4-Week Multicomponent Exercise Program on Physical Function and Body Composition in Older Adults: A Non-Randomised Controlled Trial
This study evaluated the effects of a four-week supervised multicomponent exercise program on physical function and body composition in older adults. Participants were allocated non-randomly to an intervention group or a control group based on their ability to attend the scheduled training sessions. The intervention group completed eight supervised 30-minute exercise sessions over four weeks, while the control group maintained their usual daily activity and did not begin a new exercise program. Physical function, muscle strength, gait, static balance, body mass, and body composition were assessed at baseline and after four weeks.
Studieoversikt
Status
Intervensjon / Behandling
Detaljert beskrivelse
This prospective, non-randomised controlled intervention study investigated the effects of a short-term multicomponent exercise program in older adults. Participants were allocated to either an intervention group or a control group according to their ability to attend the scheduled training sessions, primarily based on logistical factors such as place of residence and travel feasibility.
The intervention consisted of eight supervised 30-minute training sessions performed twice weekly for four weeks. The program included exercises targeting muscle strength, mobility, balance, coordination, and functional performance. Exercise volume was progressively increased during the second half of the intervention by increasing the number of repetitions and sets.
The control group received no additional exercise intervention and was instructed to maintain usual daily activity and not initiate a new exercise program during the study period. Assessments were performed at baseline and after four weeks and included muscle strength, functional mobility, gait, static balance, body mass, and body composition.
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
-
Gorzów Wielkopolski, Polen, 66-400
- Poznan University of Physical Education, Faculty of Sport Sciences in Gorzow Wielkopolski
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
Age 55-90 years Ability to ambulate independently without assistance from another person Ability to complete the full study protocol, including baseline and final assessments and, for the intervention group, participation in the four-week exercise program Provision of written informed consent
Exclusion Criteria:
Medical contraindications to physical exertion Cardiovascular, respiratory, neurological, or musculoskeletal conditions that could prevent safe performance of the tests or exercises Musculoskeletal injury or surgery within the previous six months Substantial balance or gait impairments requiring continuous assistance from another person Cognitive impairment preventing comprehension of instructions
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Multicomponent Exercise
Participants completed a four-week supervised multicomponent exercise program consisting of eight 30-minute sessions performed twice weekly. |
A supervised four-week multicomponent exercise program comprising eight 30-minute sessions performed twice weekly. The program included handgrip squeezing with a soft ball, hip flexion with a resistance band, glute bridges, single-leg stance with multidirectional reaching, supine trunk rotation, cervical spine mobility exercises, and stepping over an obstacle. The program was divided into two stages, with progression during weeks 3-4 achieved by increasing the number of repetitions and sets. |
|
Ingen inngripen: Control
Participants received no additional exercise intervention between assessments and were instructed to maintain their usual daily activity levels and not begin a new exercise program. |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Handgrip Strength
Tidsramme: Baseline to 4 weeks
|
Change in mean bilateral handgrip strength measured with a digital hand dynamometer, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Isometric Hip Flexion Strength
Tidsramme: Baseline to 4 weeks
|
Change in mean bilateral isometric hip flexion strength measured using an EasyForce dynamometer, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Isometric Hip Extension Strength
Tidsramme: Baseline to 4 weeks
|
Change in mean bilateral isometric hip extension strength measured using an EasyForce dynamometer, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Timed Up and Go Test Time
Tidsramme: Baseline to 4 weeks
|
Change in time required to complete the Timed Up and Go test, expressed in seconds. |
Baseline to 4 weeks
|
|
Change in Step Length
Tidsramme: Baseline to 4 weeks
|
Change in mean bilateral step length measured using the Zebris FDM-THQ instrumented treadmill, expressed in cm. |
Baseline to 4 weeks
|
|
Change in COP Sway Area
Tidsramme: Baseline to 4 weeks
|
Change in center-of-pressure sway area measured during 30-second quiet standing using a dual-plate posturographic platform, expressed in mm². |
Baseline to 4 weeks
|
|
Change in Body Mass
Tidsramme: Baseline to 4 weeks
|
Change in body mass measured using bioelectrical impedance analysis, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Estimated Muscle Mass
Tidsramme: Baseline to 4 weeks
|
Change in estimated muscle mass measured using bioelectrical impedance analysis, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Fat Mass
Tidsramme: Baseline to 4 weeks
|
Change in fat mass measured using bioelectrical impedance analysis, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Bone Mass
Tidsramme: Baseline to 4 weeks
|
Change in estimated bone mass measured using bioelectrical impedance analysis, expressed in kg. |
Baseline to 4 weeks
|
Samarbeidspartnere og etterforskere
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- AWF-SENIORS-44024
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
De-identified individual participant data underlying the reported results are available from the corresponding author upon reasonable request.
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .