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Dynamic Creative Arts Group Intervention to Alleviate Loneliness and Support Well-Being in Older Adults With Cognitive Changes (Dynamic-Arts)

2026年11月9日 更新者:Debbie Rand、Tel Aviv University

Alleviating Loneliness, Preserving Well-Being and Quality of Life: Immediate and Long-Term Effects of a Dynamic Creative Arts Group Intervention for Older Adults With Subjective and Mild Cognitive Impairment

The goal of this study is to investigate whether a dynamic group intervention that combines conversation and creative arts can reduce loneliness and support well-being and quality of life among older adults experiencing subjective or mild cognitive impairment.

The study will also explore how participants connect with one another, express emotions, and develop relationships during the group sessions.

Fifty older adults aged 65 and older, with subjective or mild cognitive impairment, will take part in the study.

Participants will:

Attend 10-group sessions that combine open conversations combined with creative arts, such as art, music, movement, and drama. Group sessions will be video-recorded to help researchers study participants' interactions and processes in the group.

Complete questionnaires about loneliness, well-being, and quality of life at Baseline, Pre, Post the intervention and follow-up.

Answering questions about how they feel before and after selected sessions.

Participate in an interview and share their experiences of participating in the group.

Researchers will also observe group interactions to better understand how relationships and emotional expression develop during the sessions.

研究概览

详细说明

Older adults experiencing early cognitive decline may face challenges that go beyond memory difficulties. Changes in word-finding, communication, and thinking may affect their confidence, social participation, and relationships with others. Some may feel embarrassed, become less involved in social activities, or find it difficult to share their concerns and emotions. These experiences may contribute to loneliness and reduced psychological well-being and quality of life.

At this early stage of cognitive decline, many older adults continue to live independently and maintain their everyday activities. However, they may experience uncertainty about the changes they notice and worry about the future. Opportunities for meaningful relationships, emotional expression, and a sense of belonging may be especially important during this period.

Most existing interventions for older adults with subjective or mild cognitive impairment focus on maintaining or improving cognitive abilities. Less attention has been given to their emotional and interpersonal needs, particularly the need to share personal experiences, feel understood, and develop meaningful connections with others.

A dynamic group intervention may provide an opportunity to address these needs through sharing emotions, exploring interpersonal relationships, and interacting with others in the here and now. However, difficulties with verbal expression and reflection may make participation in traditional dynamic groups challenging for some older adults with cognitive decline.

Integrating creative arts into a dynamic group offers additional ways to communicate, express emotions, and connect with others. Visual art, music, movement, and drama can support participation without relying solely on words. The creative activities are not the main therapeutic focus but serve as a way to encourage emotional expression, shared experiences, and interpersonal connections.

Study Design and Procedures

The study uses a repeated-measures design without a separate control group. Fifty participants will take part in five rounds of groups with ~10 participants per group.

Assessments will take place at four time points: baseline, approximately one month before, pre-intervention, post-intervention and follow-up, four weeks later.

The period before the intervention will serve as a comparison period to examine changes that occur without the group intervention.

Immediate psychological well-being will also be assessed before and after sessions # 2, 4, 7, and 9.

Understanding Emotional and Interpersonal Processes In addition to examining changes in loneliness, psychological well-being, and quality of life, the study will explore how participants engage with others and express emotions during the group sessions.

All sessions will be video-recorded. Selected video segments will be analyzed to identify emotional behaviors and interpersonal interactions, including facial expressions, tone of voice, gestures, body movements, and verbal communication.

The study will also examine group engagement and perceived group support, and explore whether these processes are associated with changes in loneliness and psychological well-being.

Participants' Experiences Following the intervention, individual interviews will explore participants' experiences, including meaningful moments, relationships with other group members, emotional expression, and feelings of belonging.

The study aims to better understand not only whether this intervention can support older adults with early cognitive decline, but also how emotional expression and interpersonal connections may contribute to their well-being.

研究类型

介入性

注册 (估计的)

50

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Noga Avni Orenstein, Doctoral student
  • 电话号码:+972544433773
  • 邮箱:nogaavni@gmail.com

研究联系人备份

学习地点

      • Kfar Saba、以色列
        • Azar Savion Day Center
        • 接触:
          • Efrat Occupational Therapiest, BA
          • 电话号码:+972526403186
          • 邮箱:eg@savionkfs.org

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

65年 及以上 (年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. age 65 or older
  2. who live in the community
  3. independent or need only supervision in basic activities of daily living
  4. with sufficient communicative and expressive abilities in Hebrew to allow them to participate in the group.
  5. with intact or corrected hearing and vision
  6. With Subjective or Mild Cognitive Impairment.
  7. scorse in the Montreal Cognitive Assessment (MoCA) 20 and above.

Exclusion Criteria:

1) Participants with scores ≤ 19 in the MoCA, will not be included.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Dynamic Creative Arts Group Intervention

The intervention consists of 10 sessions, held twice a week, in closed groups of 8-10 older adults with subjective or mild cognitive impairment. Each session lasts 90 minutes and includes an opening check-in, a warm-up activity, a semi-structured creative activity followed by dynamic group discussion, and a closing ritual. Creative arts, including visual art, music, movement, and drama, are used to support emotional expression and interpersonal connections. Sessions address personal identity, meaningful relationships, family, life experiences, group belonging, and separation. The facilitator encourages participants to share experiences, explore emotions, respond to one another, and reflect on relationships within the group. The intervention emphasizes here-and-now interactions, mutual support, and the development of meaningful connections.

A dynamic group intervention integrating creative arts for older adults with subjective or mild cognitive impairment. The intervention includes 10 sessions, held twice weekly, lasting 90 minutes each. Sessions combine group discussions with visual art, music, movement, and drama. The therapeutic focus is on here-and-now interactions, emotional expression, interpersonal learning, and the development of meaningful relationships. Creative activities provide additional verbal and nonverbal ways to communicate, share experiences, and connect with others. The facilitator encourages mutual support, reflection, and a sense of belonging within the group.

其他名称:
  • Dynamic group with creative arts

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
changes in scores of the Three-Item Loneliness Scale
大体时间:Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up

Perceived loneliness will be assessed using the Three-Item Loneliness Scale . The scale measures how often participants feel a lack of companionship, left out, or isolated from others. Each item is rated on a 3-point scale (1 = Hardly Ever, 2 = Some of the Time, 3 = Often). Total scores range from 3 to 9, with higher scores indicating greater perceived loneliness. The questions will be read aloud to participants.

Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up

次要结果测量

结果测量
措施说明
大体时间
changes in the lubben social network scale
大体时间:Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up

Social interaction will be measured by the Lubben Social Network Scale . This is a short measure of social isolation and perceived social support in older adults . It includes three items assessing kinship (family) ties and three items of nonkin (friendship) ties. Scores range from 0-30. A clinical cut off score of less than 12 indicates risk for social isolation.

Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up
changes in the Actual social interaction
大体时间:Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up

A non-formal observation will focus on actual social interaction of the participants. Verbal and nonverbal behaviors, engagement with other members of the center or staff will be considered Social interaction.

Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up
changes in the Positive and Negative Affect Schedule short form
大体时间:Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up

A 10 item self-report measure of positive and negative affect, representing the affective component of subjective well-being. Items are rated from 1-never to 5-always, with separate scores for positive and negative affect (range: 5-25), with higher scores indicating greater levels of the specific affect.

Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up
changes in Satisfaction With Life Scale
大体时间:Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up

The Satisfaction With Life Scale is a self-report measure, assessing global life satisfaction. Each of the 5 items is rated on a 7 point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree), total scores range from 5-35, higher scores indicate better life satisfaction.

Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up
changes in the utilization of health services
大体时间:Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up

The number of doctor visits or general visits to primary care clinic within the last two weeks (collected by self-report ).

Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up
changes in the Subjective Health Rating
大体时间:Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up

The question asked is: "In general, would you say your health is: excellent/very good/good/fair/poor?". This single item, self-rated, health measure is widely used in older adults studies and has demonstrated strong validity.

Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up
changes in the Bath Assessment of Subjective Quality of Life in Dementia
大体时间:Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up

Subjective quality of life will be assessed using the Bath Assessment of Subjective Quality of Life in Dementia . This 14-item self-report questionnaire assesses two domains: life satisfaction and feelings of positive quality of life. Items are rated on a 5-point scale from 0 to 4. Scores are transformed to a 0-100 scale, with higher scores indicating better subjective quality of life.

Baseline, pre-intervention ( 4 weeks after Baseline), post-intervention (5 weeks later) - and 4-week follow-up
changes in the immediate psychological wellbeing
大体时间:The intervention will include 10 group sessions, each session 60-90 minutes long, (twice a week). Outcome will be measured before and after sessions 2, 4, 7 and 9 .

The Canterbury Wellbeing Scale is a short, self-report, visual analogue scale to assessing subjective wellbeing 'in the moment' of people with cognitive decline. It consists of five subscales (happy/sad, well/unwell, interested/bored, confident/not confident, optimistic/not optimistic) rated 0-100, with a total score ranging from0 to 500). Higher scores means better wellbeing.

The intervention will include 10 group sessions, each session 60-90 minutes long, (twice a week). Outcome will be measured before and after sessions 2, 4, 7 and 9 .
changes in the perceived Group Processes
大体时间:The intervention will include 10 group sessions, each session 60-90 minutes long (twice a week). Outcome will be measured after sessions 2, 4, 7 and 9.

Perceived group processes will be assessed using a 7-item questionnaire developed for this study, based on existing measures of group cohesion, therapeutic alliance, and Yalom's therapeutic factors in group psychotherapy. The questionnaire assesses participants' perceptions of relationships with other group members and the facilitator, emotional sharing, interpersonal learning, and sense of belonging. Each item is rated on a 5-point agreement scale, from strongly disagree (1) to strongly agree (5). Higher scores indicate more positive perceptions of group processes.

The intervention will include 10 group sessions, each session 60-90 minutes long (twice a week). Outcome will be measured after sessions 2, 4, 7 and 9.

其他结果措施

结果测量
措施说明
大体时间
Demographic and functional data
大体时间:Baseline

A study-specific questionnaire will collect demographic and functional information, including age, sex, country of birth, marital status, education, living arrangements, and previous occupation. Additional questions address self-reported vision, hearing, mobility, independence in basic activities of daily living, and using formal care support. Two questions assess subjective memory decline and related concerns.

Baseline
The Montreal Cognitive Assessment
大体时间:baseline

The assessment will be used as an objective cognitive screening tool; scores of 26 and above will indicate Subjective Cognitive Impairment, whereas scores ranging from 19-25 will be considered Mild Cognitive Impairment and scores of 18 and below will be considered severe cognitive deficit.

baseline
Participant Satisfaction and Perceived Benefits of the Group Intervention
大体时间:At post-intervention (following completion of 10-sessions, each session 60-90 minutes long).

Participant satisfaction and perceived benefits will be assessed using a questionnaire developed for this study. It includes 13 items rated on a 5-point scale, assessing overall satisfaction, comfort with emotional sharing, perceived changes in mood and confidence, sense of belonging, interpersonal connections, perceived reduction in loneliness, facilitator support, and the contribution of creative arts to emotional expression. Additional open-ended questions explore participants' experiences, preferences, and suggestions for improvement.

At post-intervention (following completion of 10-sessions, each session 60-90 minutes long).

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年10月19日

初级完成 (估计的)

2028年5月1日

研究完成 (估计的)

2028年5月1日

研究注册日期

首次提交

2026年10月28日

首先提交符合 QC 标准的

2026年11月9日

首次发布 (实际的)

2026年11月12日

研究记录更新

最后更新发布 (实际的)

2026年11月12日

上次提交的符合 QC 标准的更新

2026年11月9日

最后验证

2026年10月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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