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Validity and Reliability of the Turkish Form of the Enjoyment of Physical Activity Scale-8 in Geriatrics With Minimal Cognitive Impairment

2026年5月14日 更新者:Gulfidan Tokgoz、Istanbul University - Cerrahpasa

Validity and Reliability of the Turkish Form of the Enjoyment of Physical Activity Scale-8 (PACES-8) in Geriatric Individuals With Minimal Cognitive Impairment

The main objective of this study is to examine the validity and reliability of the Turkish form of the Enjoyment of Physical Activity Scale-8 (PACES-8) in individuals aged 65 and over with Minimal Cognitive Impairment (MCI).

研究概览

地位

尚未招聘

详细说明

While the psychometric properties of PACES-8 have been examined in various populations in the current literature, data on its validity and reliability in geriatric individuals with Minimal Cognitive Impairment (MCI) are limited. This gap highlights a significant research need to accurately analyze the motivational determinants of physical activity behavior in elderly individuals with cognitive fragility and to make intervention programs more effective. Therefore, evaluating the validity and reliability of PACES-8 in geriatric individuals with MCI will make a significant contribution to both clinical practice and research.

研究类型

观察性的

注册 (估计的)

100

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

学习地点

      • Balıkesir、土耳其(türkiye)
        • Balıkesir University
        • 接触:
        • 副研究员:
          • Bilal Katipoğlu
        • 副研究员:
          • Ebru Tekin

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

是的

取样方法

概率样本

研究人群

Geriatric individuals aged 65 and over who meet the inclusion criteria for the study.

描述

Inclusion Criteria:

  • Being 65 years of age or older,
  • Having a diagnosis of Minimal Cognitive Impairment (MCI),
  • Having a Standardized Mini Mental Test (SMMT) score between 24 and 27 (mild cognitive impairment level),
  • Being largely independent in daily living activities (absence of functional dependency),
  • Being able to mobilize independently,
  • Having the communication level to understand and answer the survey questions,
  • Volunteering to participate in the study and providing written informed consent.

Exclusion Criteria:

  • Diagnosis of dementia or advanced cognitive impairment,
  • Acute medical conditions that prevent participation in physical activity,
  • Severe vision or hearing loss,
  • Presence of neurological or psychiatric disorders that prevent completion of questionnaire forms,
  • Serious neurological event within the last 6 months (stroke, traumatic brain injury, etc.).

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

队列和干预

团体/队列
干预/治疗
Geriartric Indivıduals with MCI
The study population will consist of individuals aged 65 and over who have been diagnosed with Minimal Cognitive Impairment.
Data will be collected after a controlled intervention representing participants' routine physical activity habits. Following the protocol implemented by Çınar-Medeni et al. (2025), participants will be asked to perform a 15-minute moderate-intensity walk (followed by a talk test). Immediately after the activity, the PACES-8 scale will be administered to measure participants' immediate enjoyment levels. To determine test-retest reliability, the PACES-8 scale will be re-administered to 20% of participants (approximately 20 people) 15 days after the initial measurement.

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
Physical Activity Enjoyment Scale-8 (PACES-8):
大体时间:1 week
This is an 8-item scale originally developed by Mullen et al. (2011) and validated in Turkish in adults by Çınar-Medeni et al. (2025). The scale uses a 7-point Likert-type format, with each item scored from 1 (did not enjoy it at all) to 7 (enjoyed it very much). The total score ranges from a minimum of 8 to a maximum of 56, with higher scores indicating greater enjoyment of physical activity.
1 week

次要结果测量

结果测量
措施说明
大体时间
International Physical Activity Questionnaire-Short Form (IPAQ-SF):
大体时间:1 week
This questionnaire will be used for criterion validity analysis. The IPAQ-SF assesses self-reported vigorous, moderate, and walking physical activity durations over the past 7 days (Öztürk, 2005). Total physical activity level is calculated in MET-minutes/week, with higher scores indicating greater levels of physical activity. The minimum possible score is 0 MET-minutes/week, and there is no fixed maximum, as scores are continuous and vary based on activity duration and intensity.
1 week

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:Bilal Katipoğlu、Yıldırım Beyazıt Universty

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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5月15日

初级完成 (估计的)

2026年6月15日

研究完成 (估计的)

2026年8月1日

研究注册日期

首次提交

2026年5月9日

首先提交符合 QC 标准的

2026年5月9日

首次发布 (实际的)

2026年5月15日

研究记录更新

最后更新发布 (实际的)

2026年5月18日

上次提交的符合 QC 标准的更新

2026年5月14日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • 2026/42

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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