Talk2gether Program for Social Connection in Older Adults
2026年8月19日 更新者：Jason Burnett、The University of Texas Health Science Center, Houston
Talk2gether Program
The purpose of this study is to see if it is feasible to recruit and retain older adults in a, weekly phone call program delivered through the Harris County Precinct 2 Healthcare and Social Services Team and to see how participation in the program affect older adults' loneliness, social isolation, psychological well-being, and satisfaction, and what barriers or challenges arise during implementation
研究概览
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：Jason Burnett, PhD
- 电话号码：(713) 873-4685
- 邮箱：Jason.Burnett@uth.tmc.edu
研究联系人备份
- 姓名：Jordan Broussard
- 电话号码：713 500 0321
- 邮箱：Jordan.Broussard@uth.tmc.edu
学习地点
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Texas
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Houston、Texas、美国、77030
- The University of Texas Health Science Center at Houston
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接触：
- Jason Burnett, PhD
- 电话号码：713-873-4685
- 邮箱：Jason.Burnett@uth.tmc.edu
-
接触：
- Jordan Broussard
- 电话号码：(713) 500-0321
- 邮箱：Jordan.Broussard@uth.tmc.edu
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-
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
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- able to provide informed consent
- able to speaks English or Spanish
- able to hear sufficiently using the telephone
Exclusion Criteria:
- Need for another person to consent on the participant's behalf
- suspected or confirmed decision-making capacity impairments
- uncontrolled psychiatric illnesses such as schizophrenia, paranoia, delusion, or delirium
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：支持治疗
- 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 |
|---|---|
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实验性的：Talk2gether program
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Participants will be paired with a trained team member.
The team member will then initiate contact with the older adult(s) to begin 90 days of weekly social calls.
These weekly social calls will be mostly unstructured, but supported by resource and conversation guides.
At the end of 90 days, if the older adult wishes to continue to receive calls, that request will be accommodated
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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 |
|---|---|---|
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Program Feasibility as assessed by number of participants recruited
大体时间：end of intervention (90 days after baseline)
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end of intervention (90 days after baseline)
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Program Feasibility as assessed by number of participants that adhered to the weekly calls
大体时间：end of intervention (90 days after baseline)
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end of intervention (90 days after baseline)
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Feasibility as assessed by number of participants that completed the program
大体时间：end of intervention (90 days after baseline)
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end of intervention (90 days after baseline)
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Feasibility as assessed by number of participants that encountered barriers or challenges as assessed by the Client Satisfaction Questionnaire (CSQ-8)
大体时间：end of intervention (90 days after baseline)
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This is an 8 item questionnaire and Items 2, 4, 5, and 8 are reverse scored.
Total scores range from 8 to 32, with the higher number indicating greater satisfaction
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end of intervention (90 days after baseline)
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Feasibility as assessed by number of participants that encountered barriers or challenges as reported on the Caller and Older Adult feedback form
大体时间：end of intervention (90 days after baseline)
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end of intervention (90 days after baseline)
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Change in social connectedness as assessed by the Lubben Social Network Scale-6
大体时间：baseline, post-intervention (Day 90)
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This is a 6-item self-report measure assessing perceived social support and social network size from family and friends.
Each item is scored from 0 to 5, and total scores range from 0 to 30.
Higher scores indicate greater social connectedness and lower risk of social isolation
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baseline, post-intervention (Day 90)
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Change in loneliness as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Social Isolation scale
大体时间：Baseline, end of intervention (90 days)
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This is an 8 item scale.
Each item is rated on a 5-point scale from 1(never) to 5 ( always).
Raw scores range from 8 to 40 and are converted to PROMIS T-scores, with a mean of 50 and standard deviation of 10 in the reference population.
Higher scores indicate greater perceived social isolation/loneliness.
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Baseline, end of intervention (90 days)
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Change in depressive symptoms as assessed by the Patient Health Questionnaire-2
大体时间：Baseline, end of intervention (90 days)
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This is a 2-item self-report measure .
Each item is scored from 0 (not at all) to 3 (nearly every day).
Total scores range from 0 to 6, with higher scores indicating greater depressive symptom burden.
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Baseline, end of intervention (90 days)
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Change in signs of elder mistreatment as assessed by the Elder Mistreatment Screening and Response Tool (EM-SART).
大体时间：Baseline, end of intervention (90 days)
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This is a 3 item questionnaire and each will be scored as either 1(yes) or 0(no) for a maximum score of 3. Higher scores or more endorsed concerns indicate a greater number of signs suggestive of elder mistreatment
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Baseline, end of intervention (90 days)
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Change in sense of purpose using the 7-item Ryff Purpose in Life Scale.
大体时间：Baseline, end of intervention (90 days)
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This is a 7 item questionnaire and each item is rated on a Likert-type scale, commonly from 1(strongly disagree) to 6( strongly agree).
Negatively worded items are reverse scored, and item scores are summed to generate a total score.
Total scores range from 7 to 42, with higher scores indicating a greater sense of purpose in life.
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Baseline, end of intervention (90 days)
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Client satisfaction as assessed by the Client Satisfaction Questionnaire
大体时间：end of intervention (90 days)
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This is an 8 item questionnaire.
Scores are summed across items once.
Items 2, 4, 5, and 8 are reverse scored.
Total scores range from 8 to 32, with the higher number indicating greater satisfaction
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end of intervention (90 days)
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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。
调查人员
- 首席研究员：Jason Burnett, PhD、The University of Texas Health Science Center, Houston
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8月3日
初级完成 (估计的)
2028年8月3日
研究完成 (估计的)
2028年8月3日
研究注册日期
首次提交
2026年8月19日
首先提交符合 QC 标准的
2026年8月19日
首次发布 (实际的)
2026年8月24日
研究记录更新
最后更新发布 (实际的)
2026年8月24日
上次提交的符合 QC 标准的更新
2026年8月19日
最后验证
2026年8月1日
更多信息
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.