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Tests mindfulness with thinking and movement training for Parkinson's and mild memory problems

Tests mindfulness with dual-task training in people with Parkinson's and mild memory problems.

Plain-language title generated from the registry record
Registry title: Mindfulness-Enhanced Dual-Task Training in PD-MCI

Key facts

Where
Nanjing, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 55 and 75 years old?

Source: NCT06930742, who can take part

Where in China

  • Nanjing Mingzhou Rehabilitation HospitalNanjing, ChinaNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Nanjing Mingzhou Rehabilitation Hospital
Trial code
NCT06930742
Record updated
16 April 2025
Original description
The goal of this clinical trial is to learn if Mindfulness-Enhanced Dual-Task Training work to treat PD-MCI in adults. The main questions it aims to answer are:Read full original descriptionShow less

Mindfulness-Enhanced Cognitive-Motor Dual-Task Training Using Balance and Isokinetic Systems for Parkinson's Disease With Mild Cognitive Impairment: A Randomized Controlled Trial

The goal of this clinical trial is to learn if Mindfulness-Enhanced Dual-Task Training work to treat PD-MCI in adults. The main questions it aims to answer are:

Does Mindfulness-Enhanced Dual-Task Training improve the cognitive or motor function of participants? Can the combination of Dual-Task Training and Mindfulness achieve better effects?

Researchers will compare 3 groups (Dual-Task Training + Mindfulness, Dual-Task Training, and conventional motor task training) to see if Dual-Task Training and Mindfulness works to treat PD-MCI.

Participants will:

Receive treatment for 4 weeks Receive scale and instrument testing before and after treatment

Inclusion: Age: Between 55 and 75 years; Disease Diagnosis: Clinically diagnosed with Idiopathic Parkinson's Disease (PD) according to the UK Parkinson's Disease Society Brain Bank Criteria; Disease Stage: Hoehn \& Yahr (H\&Y) stages 1 to 2.5; Cognitive Function: Montreal Cognitive Assessment (MoCA) score between 23 and 26, indicating mild cognitive impairment (MCI); Medication Stability: Stable doses of antiparkinsonian medications for at least 4 weeks prior to screening; Subjective Cognitive Complaints: Self-reported or informant-reported cognitive decline persisting for at least 6 months; Ambulatory Ability: Able to walk independently, with or without assistive devices; Sensory Abilities: Adequate vision and hearing to comply with study procedures; Informed Consent: Willingness to provide written informed consent and comply with study requirements.

Exclusion: Other Neurological Disorders: Presence of other neurological conditions that could affect cognitive function, such as Alzheimer's disease, stroke, or brain tumors; Psychiatric Conditions: Severe psychiatric disorders, including major depressive disorder or schizophrenia; Substance Abuse: Recent history of drug or alcohol abuse; Serious Medical Conditions: Uncontrolled hypertension, diabetes, heart disease, or other conditions that could interfere with study participation or outcomes; Severe Cognitive Impairment: Diagnosis of Parkinson's Disease Dementia (PDD); Other Factors Affecting Cognition: Recent head trauma, uncontrolled thyroid dysfunction, vitamin B12 deficiency, or other conditions known to affect cognitive function; Deep Brain Stimulation (DBS): History of DBS treatment. Participation in Other Clinical Trials: Participation in another clinical trial that could interfere with this study within the last 3 months.

ClinicalTrials.gov NCT06930742