NCT07611578Toboroz
Dual Tasking Training to Enhance Self-Efficacy in Individuals With Parkinson's Disease
Enhancing Self-Efficacy in Individuals With Parkinson's Disease Through Dual Task Training: Effects of Task Modality, Attentional Prioritization, and Cognitive Status
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. okt. 30.
Rövid összefoglaló (regiszter, angolul)
Parkinson's disease (PD) is a neurodegenerative disorder characterized by motor and cognitive impairments that substantially reduce functional independence, social participation, and quality of life. A key psychosocial factor affected by these impairments is self-efficacy, defined as an individual's belief in their ability to successfully perform tasks and achieve personal goals. In people with PD, reduced self-efficacy is closely associated with motor dysfunction, cognitive decline, fear of falling, depressive symptoms, and decreased motivation for physical and social activities. These factors interact in a bidirectional manner, creating a negative cycle in which poor confidence limits participation, further accelerating functional deterioration. From a neurophysiological perspective, the degeneration of dopaminergic neurons in PD disrupts the automatic control of movement. As a consequence, individuals with PD rely more heavily on cognitive and attentional resources to execute daily motor activities. This reliance becomes particularly problematic in dual-tasking situations, where two tasks must be performed simultaneously, such as a motor task combined with a cognitive task or two concurrent motor tasks. Because attentional capacity is limited, dividing attention across tasks frequently results in performance declines in one or both tasks, a phenomenon referred to as dual-task interference or dual-task cost. Low confidence when facing these situations may reinforce avoidance behaviors, thereby further diminishing physical activity and community engagement. Dual-task training has been proposed as a rehabilitation strategy to improve functional performance, self-efficacy, and daily functioning in people with PD. However, important gaps remain in the evidence. It is currently unclear whether motor-cognitive or motor-motor dual-task training is more effective, particularly when considering the presence or absence of cognitive impairment. Additionally, the relative impact of secondary cognitive versus secondary motor tasks on primary motor task performance has not been well established. Another unresolved issue concerns attentional prioritization strategies during dual-task training. Fixed-priority strategies require individuals to attend equally to both tasks, whereas variable-priority strategies involve alternating attention between tasks. The optimal strategy for individuals with PD, especially those with cognitive deficits, remains unknown. The proposed research aims to address these knowledge gaps by systematically evaluating the effects of different dual-task training modalities and attentional prioritization strategies on self-efficacy, functional performance, and quality of life in individuals with PD, both with and without cognitive impairment. An additional objective is to investigate whether improvements in dual-task performance are associated with reduced attentional demands, as reflected by decreased activity in the prefrontal cortex, which is considered a key neural marker of cognitive load during task performance. The research program comprises two complementary studies. Study 1 is a randomized clinical trial with a factorial design stratified by cognitive status. Participants with PD will be randomly assigned to one of four intervention groups combining dual-task modality (motor-cognitive or motor-motor) with attentional strategy (fixed-priority or variable-priority). All participants will undergo baseline assessments conducted by an interdisciplinary team of researchers. Baseline assessments include sociodemographic (age, gender, educational level, occupation), physical (weight, height) and clinical (stage of the disease, motor subtype, medication and cognitive screening measured with the Montreal cognitive assessment). Participants will complete 24 individualised training sessions over an eight-week period. Outcome measures include self-efficacy, motor and cognitive performance, quality of life, dual-task cost, and prefrontal cortex activity. Study 2 uses a cross-sectional design that includes individuals with PD from study 1 and a matched group of healthy older adults. Using identical assessment procedures, this study compares dual-task interference and prefrontal cortex activity between people with PD and healthy controls, providing additional insight into disease-specific cognitive-motor interactions. Overall, this research seeks to inform evidence-based, personalized rehabilitation strategies by identifying the most effective dual-task training approaches for improving confidence, functional ability, and quality of life in individuals with PD.
- Állapot (regiszter)
- Toboroz
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 112 (tervezett)
- Első benyújtás
- 2026. máj. 7.
- Kezdés
- 2026. okt. 5.
- Elsődleges befejezés
- 2029. jan. 31.
- Fő szponzor
- Alvaro Reyes
- Betegségek
- Parkinson-kór
- NCT-szám
- NCT07611578
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó
- Tervezett résztvevők: 112
- 2026. okt. 5. és az elsődleges befejezés (2029. jan. 31.) között
- 1 helyszín, 1 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.
AI-kivonat: kiket keres a vizsgálat
Gép olvasta ki az oldalon álló regiszterszövegből, ezért tévedhet. Hogy ki vehet részt, azt a lenti regiszterszöveg és a vizsgálat csapata dönti el.
A vizsgálat olyan felnőtteket keres, akiknek neurológus által megerősített idiopátiás Parkinson-kórjuk van, és önállóan tudnak járni. A gyakorlás során két feladatot végeznek egyszerre.
- Életkor
- 18 éves vagy idősebb
- Nem
- Nők és férfiak egyaránt részt vehetnek.
- A betegség stádiuma
- Hoehn–Yahr I., II. vagy III. stádium. Nincs, enyhe vagy közepes kognitív zavar. Depressziós tünetekkel vagy anélkül.
- Korábbi kezelés
- A gyógyszer adagjának és típusának változatlannak kell lennie a vizsgálat kezdete előtti 3 hónapban.
A részvétel fő kizáró okai
- Bármilyen más idegrendszeri vagy mozgásszervi betegség
- Korábbi láb- vagy agysérülés, illetve műtét
- Látás- vagy halláproblémák, amelyek befolyásolhatják a kognitív teszteket
- Orvos által megállapított súlyos neurokognitív zavar
Gépi kiolvasás: 2026. nov. 9..
Ki nem vehet részt
Szó szerint a(z) ClinicalTrials.gov forrásból, témák szerint csoportosítva. Hogy ki vehet részt, azt csak a vizsgálat csapata dönti el.
Korábbi kezelés
- The presence of any other concomitant neurological, musculoskeletal disease
Más betegség
- History of leg or brain trauma or surgery
- Clinical diagnosis of major neurocognitive disorder
Egyéb
- Vision or hearing problems that may affect the performance of cognitive tests
A regiszterben nem jelölt feltételek
- Participants diagnosed with idiopathic Parkinson's disease confirmed by a neurologist will be recruited in this study. Inclusion criteria will be:
- Hoehn \& Yahr stages I, II or III
- Participants with no or mild to moderate neurocognitive impairments
- Participants with and without symptoms of depression
- Able to walk independently
- Unaltered dose and type of medication up to three months before the commencement of the study
- Participants able to understand and respond to the instructions given in the study.
Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (1)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Facultad de Ciencias de la Rehabilitacion | Santiago | Chile | Toboroz |
Ez az oldal tájékoztatás, nem orvosi tanács. Bármely vizsgálatról az orvosoddal beszélj.