3.1. Study Design
The current descriptive, cross sectional study aimed at evaluating the validity and reliability of Persian version of the brief CSI-D in a geriatric population of Iran.
3.2. Participants
The participants were elderly people, aged 60 and above, referred to Yaadmaan Referral Center for Dementia and Cognitive Disorders in Tehran, Iran and received dementia, MCI, or SCI diagnosis by a neurologist with expertise in dementia. Of a total of 268 participants, 209 subjects had SCI, MCI, or dementia, and the remaining 53 subjects selected from the caregivers of patients in the center had normal cognition.
3.3. Interviewers
The raters were clinical psychologists trained by a neurologist with expertise in dementia to ensure that the study procedure (i e, data handling, data entry, and data analysis) is conducted properly. The raters were blind to the final diagnosis of the subjects.
3.4. Diagnostic Criteria
Dementia, MCI, and SCI were diagnosed by a neurologist with expertise in dementia according to criteria in the Persian version of Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV-IR) and the functional assessment staging of dementia of the Alzheimer’s type (FAST) after clinical examination.
3.5. Inclusion Criteria
Inclusion criteria for all participants were the age 60 and above and speaking in Persian as maternal language. The eligible participants were allocated to three groups of dementia, MCI, and SCI. The presence of an informant or caregiver informed about the subject’s daily living activities was mandatory for patients with MCI or dementia.
The control group included elderly participants without any complaint of memory loss or cognitive decline. The demographic characteristics of the control group were similar to those of the dementia group in terms of age, gender, and level of education.
3.6. Exclusion Criteria
Exclusion criteria for all participants were clinically significant depression, delirium, mental retardation, taking medication affecting cognitive functions, visual or hearing loss, speech disorder, and alcohol or substance abuse. In addition, behavioral and psychological symptoms of dementia (BPSD) interfering with neuropsychological assessments were also considered.
3.7. Test Translation and Adaptation
After getting permission from ADI, both patient and informant questionnaires were translated and back translated into Persian by experts who were fluent in both Persian and English languages and were familiar with neuropsychology tests. During the test adaptation, the two words of “Boat and Fish” in delayed recall test were changed to “Knife and Sun”, because they have a semantic similarity and belong to the same category. Since both the words boat and fish belong to the same category, the authors conclude that the subjects may be able to memorize them and, hence, they were not suitable for the delayed recall test.
All steps of translation and adaptation were conducted under the supervision of a neurologist along with neuropsychological assessments.
3.8. Data Collection
The interviewers gathered the subject’s main demographic data such as age, gender, handedness, and ethnicity; the educational level was determined based on the number of years of formal education.
In the patient questionnaire, delayed recall (three words), orientation, and naming were asked. The total score was obtained by summing the scores across items of each question (ranged 0 - 9). Based on test instruction, taking informant questionnaire was not applicable for the subjects who obtained 0 - 4 (dementia) and 8 - 9 (normal) scores. The informant questionnaire was completed by the companions whose patients scored 5 to 7 in the patient questionnaire.
In the informant questionnaire, six questions were asked about subjects’ memory and cognitive status (scored 0 - 6).
Before CSI-D administration, the neurologist visited all the subjects and determined the final diagnosis based on clinical examination and para-clinical findings including laboratory tests, magnetic resonance imaging, etc.
3.9. Ethics
All participants (or their companion or legal guardian) signed the informed consent form before enrollment in the study. Adequate informed about the study objectives was given to participants and they were also assured about their right to withdraw from the study at any stage. All the collected data were kept confidential and just the first author had access to them. All documents were stored in a secured place.
3.10. Statistical Analysis
The criterion validity was determined using the Spearman correlation coefficient between the Persian version of the brief CSI-D and the specialist diagnosis as the gold standard. Sensitivity and specificity of the instrument were also measured. The internal consistency was determined using Cronbach’s alpha. External reliability was determined based on the average correlation coefficient ≥ 0.8 based on the test results of two raters. The content validity was determined by the diagnosis of the neurologist.