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Intervention Group for Dementia

N/A

Waitlist Available

Led By Wen Liu, PhD

Research Sponsored by University of Kansas Medical Center

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up change from baseline to week 12

Summary

The purpose of this study is to learn the effects of two mild body exercises on quality of life, non-motor symptoms, anxiety, depression, fatigue, sleep quality, cognition, and executive function on people with Parkinson's Disease (PD).

Eligible Conditions

Dementia
Parkinson's Disease

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ change from baseline to week 12

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~change from baseline to week 12

This trial's timeline: 3 weeks for screening, Varies for treatment, and change from baseline to week 12 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Parkinson's Disease Sleep Scale (PDSS-2)

Secondary study objectives

Frontal Assessment Battery (FAB-18)

Geriatric Anxiety Scale (GAS-10)

Geriatric Depression Scale (GDS-15)

+10 more

Trial Design

2Treatment groups

Experimental Treatment

Placebo Group

Group I: Intervention GroupExperimental Treatment1 Intervention

Participation in the intervention group will involve a total of 14 visits over about 14 weeks to the study site, and then a 6-month follow-up evaluation. Participants will learn and practice the Qigong exercise during the study.

Group II: Control GroupPlacebo Group1 Intervention

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