We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

IMProving Executive Function Study (IMPRES)

This study is currently recruiting participants.
Verified September 2017 by University of Pennsylvania
Sponsor:
ClinicalTrials.gov Identifier:
NCT03187353
First Posted: June 14, 2017
Last Update Posted: September 26, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by (Responsible Party):
University of Pennsylvania
  Purpose
This is a double-blind, placebo-controlled, crossover study testing whether Vyvanse (lisdexamfetamine; LDX) improves executive functioning (EF) in 100 postmenopausal women who report onset of EF difficulties after oophorectomy. This study involves magnetic resonance imaging (MRI) to see how LDX affects brain chemistry while undergoing two 6-week trials of the study drug and placebo capsules.

Condition Intervention Phase
Cognitive Impairment RRSO Drug: Lisdexamfetamine Drug: Placebo oral capsule Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Multi-Modal Imaging of Psychostimulant Effects on Executive Function Post-RRSO

Resource links provided by NLM:


Further study details as provided by University of Pennsylvania:

Primary Outcome Measures:
  • Brown Attention Deficit Disorder Scale (BADDS) Score [ Time Frame: 6 weeks ]
    To subjectively determine whether treatment with LDX improves self-reported executive function (EF) via the BADDS


Secondary Outcome Measures:
  • Brain activation [ Time Frame: 6 weeks ]
    To objectively determine the impact of LDX on executive system activation during a working memory task via proton magnetic resonance spectroscopy (1H-MRS) and functional magnetic resonance imaging (fMRI)


Estimated Enrollment: 100
Actual Study Start Date: September 22, 2017
Estimated Study Completion Date: July 1, 2022
Estimated Primary Completion Date: July 1, 2022 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Lisdexamfetamine
Participants will have a 50% chance of receiving the active study medication. They will begin at 20 mg/d and will increase up to 60 mg/d after 4 weeks, if well tolerated. Total time on the study drug is up to 6 weeks.
Drug: Lisdexamfetamine
Stimulant medications are used to reduce interruptive behavior, fidgeting, and other hyperactive symptoms, as well as help a person finish tasks and improve his or her relationships for adults who have ADHD. Please note that the FDA has not approved the use of Vyvanse® for the treatment of memory and concentration difficulties related to medically induced menopause.
Other Name: Vyvanse
Placebo Comparator: Placebo
Participants will have a 50% chance of receiving the placebo for this study. They will begin with 1 sugar pill and will increase up to 3 pills after 4 weeks. Maximum time for taking the placebo is 6 weeks.
Drug: Placebo oral capsule
The placebo capsule will be filled with microcellulose.
Other Name: sugar pill

Detailed Description:

Following a medically induced menopause, many women report difficulty in remembering things, focusing and concentrating. The purpose of this study is to examine the effects of a stimulant medication called Vyvanse® (lisdexamfetamine; LDX) on executive functioning, such as attention, processing, organization, and memory, in women who are experiencing executive functioning difficulties after having undergone a risk-reducing bilateral salpingo-oophorectomy (RRSO). This study involves magnetic resonance imaging (MRI) to see how LDX affects brain chemistry while undergoing two 6-week trials of the study drug and placebo capsules.

Individuals wishing to participate in this study are medically healthy women between the ages of 35-55 years old who have undergone a risk-reducing bilateral salpingo-oophorectomy (RRSO) within the previous 15 years. Participants must have been premenopausal before undergoing RRSO (meaning they were having regular periods). They also must not have undergone radiation or chemotherapy at any point before or after your RRSO.

Furthermore, participants must not suffer from a mental illness, including Attention Deficit Hyperactivity Disorder (ADHD), and must not have a recent history of drug abuse. Additionally, participants must also be right-handed, not suffer from a fear of small, enclosed spaces (claustrophobia), and not have any implanted medical devices such as a pacemaker, orthodontic braces, or shrapnel. They must not have a history of seizures, uncontrolled hypertension or known renal impairment.

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   35 Years to 55 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Female;
  • Age 35-55;
  • Have undergone risk-reducing bilateral salpingo-oophorectomy (RRSO) within the previous 15 years AND were premenopausal at the time of RRSO;
  • Score of ≥ 20 on the Brown Attention Deficit Disorder Scale (BADDS);
  • Onset of executive function difficulties occurred post RRSO;
  • Right-handed;
  • Are fluent in written and spoken English;
  • Are able to give written informed consent (obtained at screening visit);
  • Have an Intelligence Quotient of at least 90 as per the Wechsler Abbreviated Scale of Intelligence (WASI) assessment.

Exclusion criteria:

  • Current, untreated psychiatric disorder;
  • Substance use disorder within the previous 3 years;
  • Lifetime history of ADHD or psychotic disorder including bipolar disorder, schizoaffective disorder, and schizophrenia;
  • Lifetime history of stimulant abuse or dependence;
  • Regular use of psychotropic medications except selective serotonin reuptake inhibitors (SSRI), serotonin noradrenergic reuptake inhibitors (SNRI), bupropion, zolpidem or gabapentin;
  • Current use of aromatase inhibitors or chemotherapies (within the past year);
  • Previous history of sensitivity or adverse reaction to lisdexamfetamine (LDX);
  • History of seizures or unstable medical condition;
  • Known heart disease or clinically significant abnormal electrocardiogram during screening as determined by the study MD; 10. Uncontrolled hypertension; 11. Presence of a metallic implant contraindicative to scanning at the 7T level; 11. Claustrophobia. 12. Consistent systolic blood pressure of >145mm Hg or diastolic blood pressure >90 mm Hg after three readings at time of screening; 13. Known renal impairment and End Stage Renal Disease (ESRD).
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03187353


Contacts
Contact: Emily A Lipner, BA 215-573-8873 lipnere@mail.med.upenn.edu
Contact: Claudia J Iannelli, MS 215-417-8839 sclaud@mail.med.upenn.edu

Locations
United States, Pennsylvania
3535 Market Street Recruiting
Philadelphia, Pennsylvania, United States, 19104
Contact: Emily Lipner    215-573-8873    lipnere@mail.med.upenn.edu   
Contact: Cynthia Neill Epperson, MD    215-573-8871    cepp@mail.med.upenn.edu   
Sponsors and Collaborators
University of Pennsylvania
Investigators
Principal Investigator: C. Neill Epperson, MD University of Pennsylvania
  More Information

Additional Information:
Publications:
Responsible Party: University of Pennsylvania
ClinicalTrials.gov Identifier: NCT03187353     History of Changes
Other Study ID Numbers: 826981
First Submitted: June 12, 2017
First Posted: June 14, 2017
Last Update Posted: September 26, 2017
Last Verified: September 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No

Keywords provided by University of Pennsylvania:
Cognitive complaints
RRSO
Oophorectomy
Memory
Cognition
Early menopause

Additional relevant MeSH terms:
Cognitive Dysfunction
Cognition Disorders
Neurocognitive Disorders
Mental Disorders
Lisdexamfetamine Dimesylate
Central Nervous System Stimulants
Physiological Effects of Drugs
Dopamine Uptake Inhibitors
Neurotransmitter Uptake Inhibitors
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Dopamine Agents
Neurotransmitter Agents