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临床试验/NCT05668481
NCT05668481已完成不适用

Improving Memory for Treatment for Patients Experiencing Mild Cognitive Impairment: Are Constructive or Non-constructive Memory Supports More Helpful?

University of California, Berkeley1 个研究点 分布在 1 个国家目标入组 119 人开始时间: 2023年5月19日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
119
试验地点
1
主要终点
Number of items recalled on the free recall task to assess outcome for non-constructive memory support

研究概览

简要总结

The main empirical question to be addressed is: What types of memory support are most potent for patients who are experiencing a mild cognitive impairment (MCI) relative to non-MCI patients?

详细描述

People experiencing mild cognitive impairment (MCI) may benefit from adding memory support to treatment-as-usual. Adding memory support may be an innovative way to improve patient memory for treatment, adherence to treatment and outcome.

The key question is: What types of memory support are most potent for MCI patients relative to non-MCI patients?

The aim of the proposed research is to assess patient memory for treatment and the impact of adding memory support for people who are and are not experiencing MCI. The investigators will also compare the effectiveness of constructive vs. non-constructive memory supports for people who are experiencing MCI compared to people who are not experiencing MCI.

Hypotheses:

  1. Recall of the content of treatment will be lower in the MCI group relative to the non-MCI group.
  2. Constructive memory support will be more effective for the non-MCI group relative to the MCI group.
  3. Non-constructive memory support will be more effective for the MCI group relative to the non-MCI group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Participant)

盲法说明

Participants will not be aware that they are receiving constructive memory support in one session and non-constructive memory support in the next session

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Participants 60 years and older will be recruited.
  • •Fluent in English.
  • •Experiencing some difficulties relating to sleep and circadian functioning and (d) a score of 19-25 on the Montreal Cognitive Assessment (for the MCI group) and score 26-30 on the Montreal Cognitive Assessment (for the non-MCI group) (e) Have a computer to use and an internet connection and (f) be able to attend sessions weekly and on the same day each week.

排除标准

  • •Presence of an active and progressive mental or physical illness or neurological degenerative disease;
  • •Night shift work >2 nights per week in the past 3 months;
  • •Not able and willing to participate in and/or complete the assessments and participate in the treatment.

研究组 & 干预措施

Constructive memory support

Active Comparator

Participants will watch videos of a sleep expert delivering treatment components from the Transdiagnostic Sleep and Circadian Intervention (TranS-C). After each video, a team member will deliver constructive memory supports.

干预措施: Transdiagnostic sleep and circadian intervention (TranS-C) (Behavioral)

Non-constructive memory support

Active Comparator

Participants will watch videos of a sleep expert delivering treatment components from the Transdiagnostic Sleep and Circadian Intervention (TranS-C). After each video, a team member will deliver non-constructive memory supports.

干预措施: Transdiagnostic sleep and circadian intervention (TranS-C) (Behavioral)

结局指标

主要结局

Number of items recalled on the free recall task to assess outcome for non-constructive memory support

时间窗: Delivered two times: At the end of the session in which non-constructive memory supports were used (baseline) and 1 week later.

Assesses patient memory for treatment

Number and accuracy of thoughts about the material covered in the prior treatment session in which constructive memory supports were delivered

时间窗: Delivered once: At the beginning of the session held 1 week after the delivery of the constructive memory supports

To assess if the participant thought about the therapy session and if the thoughts accurately reflected the prior treatment session

Number and accuracy of applications of the material covered in the prior treatment session in which non-constructive memory supports were delivered

时间窗: Delivered once: At the beginning of the session held 1 week after the delivery of the non-constructive memory supports

To assess if the participant applied the material covered in the therapy session and if the participant accurately applied the material prior treatment session

Number of items recalled on the free recall task to assess outcome for constructive memory support

时间窗: Delivered two times: At the session in which constructive memory supports were used (baseline) and 1 week later.

Assesses patient memory for treatment

Number and accuracy of thoughts about the material covered in the prior treatment session in which non-constructive memory supports were delivered

时间窗: Delivered once: At the beginning of the session held 1 week after the delivery of the non-constructive memory supports

To assess if the participant thought about the therapy session and if the thoughts accurately reflected the prior treatment session

Number and accuracy of applications of the material covered in the prior treatment session in which constructive memory supports were delivered

时间窗: Delivered once: At the beginning of the session held 1 week after the delivery of the constructive memory supports

To assess if the participant applied the material covered in the therapy session and if the participant accurately applied the material prior treatment session

次要结局

  • Acceptability of constructive memory support(One time point: At the end of the treatment session in which constructive memory support was delivered)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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