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Evaluate Healthy Lifestyle Program on cognitive outcomes for Obesity
N/A
Waitlist Available
Led By Robert M Roth, PhD
Research Sponsored by Dartmouth-Hitchcock Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline
Awards & highlights
Study Summary
This study is evaluating whether an intensive lifestyle intervention can improve cognitive functioning in older adults with obesity.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline and 17 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 17 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change from baseline Anxiety Symptoms at 17 weeks
Change from baseline Mood Symptoms at 17 weeks
Change from baseline Subjective Health Status (PROMIS) at 17 weeks
+14 moreSecondary outcome measures
Baseline estimated level of intellectual ability
Handedness as measured by Edinburgh Handedness Inventory at Baseline
Trial Design
2Treatment groups
Experimental Treatment
Group I: Sarcopenia and ObesityExperimental Treatment1 Intervention
Assess the effect of an intensive lifestyle intervention on cognitive function in adults with obesity and sarcopenia who are 65 years and older.
Group II: Obesity OnlyExperimental Treatment1 Intervention
Assess the effect of an intensive lifestyle intervention on cognitive function in adults with obesity who are 65 years and older.
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Who is running the clinical trial?
Dartmouth-Hitchcock Medical CenterLead Sponsor
524 Previous Clinical Trials
2,543,335 Total Patients Enrolled
15 Trials studying Obesity
13,956 Patients Enrolled for Obesity
Robert M Roth, PhDPrincipal InvestigatorDartmouth-Hitchcock Medical Center
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