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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 weeks
Treatment ~ Varies
Follow Up ~baseline and 17 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline and 17 weeks for reporting.

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 more
Secondary 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

Frequently Asked Questions

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~1 spots leftby Apr 2025