- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07831174
Modified Otago Exercise Program on Neurocognitive Level and Balance Parameters
The Effect of Modified Otago Exercise Program on Neurocognitive Level and Balance Parameters in Community-Dwelling Older Adults: A Randomized Controlled Trial
This study examined the effect of an eight-week modified Otago Exercise Program on neurocognitive level and balance parameters in community-dwelling older adults.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Eighty-seven individuals aged 65 years and over were assigned to an intervention group (n=43) or a control group (n=44) through block randomization.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
-
Antalya, Tyrkiet (Türkiye)
- Alanya Alaaddin Keykubat University
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Be 65 years of age or older,
- Be able to walk at least ten meters unaided or with the support of a walking aid, - Not have a diagnosed neurological or orthopedic problem affecting walking and balance,
- Not have visual or hearing impairments, and score 24 or higher on the Standardized Mini Mental State Test.
Exclusion Criteria:
- Having undergone lower extremity surgery within the last six months and being illiterate.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Otago Exercise
Otago exercise program + Daily routine |
Otago exercise + Daily routine |
|
Aktiv komparator: Control
Daily routine |
Only daily routine |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Cognitive State Test
Tidsramme: Enrollment and the end of 8 week-intervention
|
Cognitive State Test is a tool for the detailed screening of cognitive function. It is scored out of a total of thirty points. A high score corresponds to high cognitive performance. |
Enrollment and the end of 8 week-intervention
|
|
Dynamic Balance Test
Tidsramme: Enrollment and the end of 8 week-intervention
|
The Timed Up and Go Test was administered to assess dynamic balance. The time taken to complete the test was recorded; a shorter duration indicates good dynamic balance performance, whereas values exceeding 14 seconds are associated with an increased risk of falling. |
Enrollment and the end of 8 week-intervention
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Warwick-Edinburgh Mental Well-being Scale
Tidsramme: Enrollment and at the end of the 8th week
|
It consists of fourteen five-point Likert-type items and yields scores ranging from fourteen to seventy. A high score indicates a high level of mental well-being. |
Enrollment and at the end of the 8th week
|
|
Single-Leg Stance Test
Tidsramme: Enrollment and at the end of the 8th week
|
One leg is lifted without touching the supporting leg, and the individual is expected to maintain their balance for thirty seconds; the duration is recorded in seconds. |
Enrollment and at the end of the 8th week
|
Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- 2024/05
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .