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Efficacy of PDCA-based nursing intervention on activities of daily living in motor deficit patients due to neurological disorders

A Randomized Controlled Trial to evaluate the efficacy of PDCA (Plan-Do-Check-Act)-Based Nursing Interventions in improving activities of daily living among patients with motor deficits Due to neurological disorders in a selected hospital in Maharashtra - Nil

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090361
Enrollment
44
Registered
2025-07-07
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G839- Paralytic syndrome, unspecified

Interventions

Intervention1: PDCA (Plan-Do-Check-Act)-Based Nursing Interventions to improve ADL (Activities of daily living) score: Patients with motor deficit who are not able to perform ADL (Activities of daily

Sponsors

Donna Lim
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Motor Deficits - Patients exhibiting motor deficits (eg hemiparesis, paralysis, or muscle weakness) that significantly impact Activities of Daily Living (ADLs) 2. Age Adults aged 18 years and above. 3. Hospital Stay Patients admitted to the selected tertiary care hospital for treatment and rehabilitation. 4. Functional Limitation Patients experiencing difficulty in activities of daily living (ADLs) due to neurological impairment. 5. Consent - Patients who provide written informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Acute or Severe Stages of Neurological Disorders - Patients in the acute phase of a neurological event (within 72 hours of a stroke or head injury) where their condition is unstable and likely to prevent meaningful participation. 2. Severe Cognitive Impairment, Patients with severe cognitive dysfunction (such as advanced dementia, unconscious patients, or those with profound intellectual disability) who cannot follow instructions. 3. Severe Comorbidities, that is patients with life-threatening comorbid conditions (such as end-stage organ failure, advanced malignancies) that could interfere with intervention participation. 4. Psychiatric Illness - patients with psychiatric disorders (such as schizophrenia, severe depression, or active psychosis) that may affect participation in ADL-based interventions. 5. Severe Visual or Hearing Impairment: Patients with significant sensory impairments (such as blindness or profound hearing loss) that may hinder their ability to participate in rehabilitation exercises, interact with caregivers, or engage in ADL tasks.

Design outcomes

Primary

MeasureTime frame
Improvement in Activities of Daily Living (ADLs)Timepoint: 4 weeks

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDONNA LIM

College of Nursing, AFMC, Pune

cllekshmi@gmail.com7499592746

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026