Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:35 PM
Ignite Modification Date:
2025-12-24 @ 5:35 PM
NCT ID:
NCT01525368
Eligibility Criteria:
Inclusion Criteria:
* male or female patients, fulfilling Petersen´s criteria of amnestic mild cognitive impairment (aMCI)
* No evidence for other psychiatric axis I disorders according to DSM-IV criteria.
* No evidence for neurological disorders (e.g. stroke)
* No uncontrolled arterial hypertension or diabetes mellitus
* No history of drug / alcohol abuse
* The patient is able to provide written informed consent to participate in the study.
* for the cognitive-reserve-study patients, a high (low) cognitive reserve is defined as a verbal IQ score of \>/= 120 (\</= 110) as assessed by the MWT-B, a German multiple vocabulary test
Exclusion Criteria:
* Evidence for acute psychiatric or neurological disorders
* Uncontrolled arterial hypertension or diabetes mellitus
* History of drug / alcohol abuse
* No ability to participate and no willing to give informed consent and comply with the study restrictions.
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT01525368
Study Brief:
Protocol Section:
NCT01525368