SIHT-16: Free and Cued Selective Reminding Test (16-words) Turkish Adaptation Study

• Sponsor: Istanbul University (Other)
• Overall Status: Completed
• CT.gov ID: NCT05756231
• Collaborator: (none)
• Enrollment: 270
• Location: 1
• Arm: 1
• Actual Duration (Months): 37.5
• Patients Per Site Per Month: 7.2

Study Details

Study Description

Brief Summary

An Adaptation Study of Free and Cued Selective Reminding Test in Turkish

Condition or Disease	Intervention/Treatment	Phase
Dementia; Memory Impairment	Behavioral: SIHT-16	N/A

Detailed Description

As very commonly used for objectifying Alzheimer Disease memory deficits, an adaptive selection of word choices are done for the use of free and cued selective reminding test (FCSRT) procedure in Turkish population. In this study the validity and reliability of the test to measure memory deficits in persons with memory complaints will be discussed.

Study Design

• Study Type: Interventional
• Actual Enrollment: 270 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Screening
• Official Title: Free and Cued Selective Reminding Test (16-words) Turkish Adaptation Study
• Actual Study Start Date: Jan 5, 2020
• Actual Primary Completion Date: Jan 26, 2023
• Actual Study Completion Date: Feb 20, 2023

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Turkish Adaptation Study of Free and Cued Selective Reminding Test (SIHT-16) Outcomes of Turkish adaptation of Free and cued selective reminding test (SIHT-16) is compared with memory and non-memory test in three alternative lists: a,b, and c parallel lists. The participants are assessed in neurological diagnosis routine.	Behavioral: SIHT-16; a pencil-paper assessment tool.

Outcome Measures

Primary Outcome Measures

1. Validity of translation [once]

   Variances of answers given to each form will be compared to each other to know if they are similar or different.

2. Factor Analyses [once]

   Factor Analyses must be conducted to redefine the weight of each item on measuring memory deficits to be sure that turkish words version is similar to original factor weights.

3. Validity of the ability of the measure to objectify the memory deficit in dementia [once]

   Test measures must be sensitive enough to objectify a memory deficits even in early stages of dementia. The scores of memory test in early and late stages of dementia will be compared to see if they are different. It's expected to be different.

Eligibility Criteria

Criteria

• Ages Eligible for Study: N/A and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• having memory complaints

• demanding clinical consultation for the memory complaint

Exclusion Criteria:

• vascular pathology

• extrapyramidal findings

• psychiatric illness

• epilepsy

• cognition affecting drug use

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Istanbul University	Istanbul		Turkey	34340

Sponsors and Collaborators

• Istanbul University

Investigators

• Study Director: İ. Hakan Gürvit, Prof. MD., Istanbul University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Jbid DURSUN UNCU, Clinical Neuropsychologist, Istanbul University
• ClinicalTrials.gov Identifier: NCT05756231
• Other Study ID Numbers: 2019/778
• First Posted: Mar 6, 2023
• Last Update Posted: Mar 6, 2023
• Last Verified: Feb 1, 2023

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Jbid DURSUN UNCU, Clinical Neuropsychologist, Istanbul University: Alzheimer Disease; Memory Complaint; Memory; Dementia; Free and Cued Selective Reminding Test; Adaptation; Validity
• Additional relevant MeSH terms: Dementia

Study Results

No Results Posted as of Mar 6, 2023