A Study of a Memory Intervention to Improve Medicine Adherence in Patients with Mild Cognitive Impairments and Family Caregiver Medication Administration

  • Chiu, Yi-Chen (PI)
  • Chang, Ting Huan (CoPI)
  • Heh, Jia-Sheng (CoPI)
  • Hsu, Wen Chuin (CoPI)
  • Hsu, Jung Lung (CoPI)
  • Hua, Mau Sun (CoPI)
  • Lin, Chia-Hung (CoPI)

Project: National Science and Technology CouncilNational Science and Technology Council Academic Grants

Project Details

Abstract

Background and Purpose: Previous studies indicate that baseline cognitive abilities, especially prospective memory (PM) significantly influence medication adherence. However, there are only three qualified intervention studies on adherences in persons with cognitive impairment (PWCIs). In addition, family caregivers (FCGs) are often asked to assist PWCIs in managing their medication but FCGs’ medication administration hassles are not intensively investigated. Therefore, the purpose of this project is to test the effectiveness and efficacy of a theoretical-based multifaceted memory intervention on medication administration and quality of life in PWCIs living at home and medication administration hassle of their FCGs. Study Design: This is a three-year project (2015, 8, 1-2018, 7, 31). The aims of the first-year study are: 1.to develop a multifaceted memory intervention based on the paradigm of prospective memory (PM); 2. to pilot test the feasibility of the multifaceted memory intervention through a small randomized control trial. The aims of the second- to third year study are: 3. to examine the effectiveness and efficacy of the intervention (a randomized control trial). The intervention group will receive a cognitive impairment education, medication adherence and memory strategies training, while the control group will receive only the cognitive impairment education program. The duration of the intervention is one month. There will be 4 data collections (baseline, post-intervention 2 4, 6 months). Sample size estimation for the pilot study is 5 dyads for each group. Sample size for the randomized clinical trial is 84 dyads (42 dyads per group). After the attrition rate (10%) is counted, in total, there will be 200 cases (100 dyads). Implications of this project: This three-year program can help to identify those who may benefit from memory training and assist those who may be incompetent living in community. Also our program will extend the current knowledge of the role of PM playing in medication adherence behavior and its relationships with self awareness as well as everyday decision making among PWCIs. In addition, health related professionals can improve PWCI’s quality of care and reduce FCG hassle by applying a theoretical guided practice for memory training.

Project IDs

Project ID:PC10408-1520
External Project ID:MOST104-2314-B182-005
StatusFinished
Effective start/end date01/08/1531/07/16

Keywords

  • mild cognitive impairment
  • prospective memory
  • memory training

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