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临床试验/NCT07400081
NCT07400081尚未招募不适用

Effectiveness of a Community-based Intervention Programme to Promote Well-being in Older Adults

National Healthcare Group Polyclinics1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2026年3月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
300
试验地点
1
主要终点
Well-being

研究概览

简要总结

This study is conducted to assess the effectiveness of a community intervention programme on improving well-being, levels of distress, and loneliness in older adults (aged 55 years old and above), who have symptoms of depression.

Social Service Agencies (SSAs) will conduct focal talks on well-being for the community. As part of the focal talks, the Public Health Questionnaire-9 (PHQ-9) will be conducted. Attendees with a PHQ-9 score of 1-9 will be invited to take part in the study. Up to 300 participants will be recruited and randomised into 2 arms: control arm (150 participants) and intervention arm (150 participants).

Participants in the intervention arm will undergo 8-week community intervention programme which includes 4 sessions on well-being and continuous follow-up with a Health Companion. Participants in the control arm will be offered to join a programme conducted by the SSAs 8 weeks after recruitment into the study. The programmes offered to the control group are independent of the study.

详细描述

Study Procedures:

Control arm: Participants randomised into the control arm will not be offered any programmes for 8 weeks after their recruitment into the study. After 8 weeks, the SSAs will offer the participants an intervention programme that is independent of the study.

Intervention arm: Participant in the intervention arm will undergo 4 face-to-face, group psychoeducation sessions, conducted fortnightly over a period of 8 weeks. The sessions will teach the participants about well-being and share with them strategies to improve their well-being. Health Companions from the SSAs will conduct check-ins with the participants over the phone, and recommend some nearby activities for them.

Methods and assessments:

Questionnaires including the 6-item De Jong Gierveld Loneliness Scale, Warwick-Edinburgh Mental Wellbeing Scale, Patient Health Questionnaire-9, and Generalised Anxiety Disorder-7 at the baseline and endpoint for all participants.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Aged 55 and above
  • Score of 1-9 on the PHQ-9 questionnaire
  • Able to speak and understand English, Chinese or Malay
  • Able to provide informed consent
  • Be willing to use common technologies (such as phone calls, texting via SMS/whatsapp) for communication

排除标准

  • PHQ-9 score of 0
  • PHQ-9 score of 10 or more
  • Actively being followed up by a mental health professional
  • On psychotropic medication or are undergoing psychotherapy
  • Have other mental disorders or are suicidal
  • Have physical difficulties, cognitive impairment or difficulties with speech, sight and hearing or mobility that may prevent their engagement in activities

研究组 & 干预措施

Control

No Intervention

Waitlist Control

Intervention

Other

Community-based Intervention

干预措施: Community-based Intervention (Behavioral)

结局指标

主要结局

Well-being

时间窗: 8 weeks

Measured by Warwick-Edinburgh Mental Well-being Scale (WEMWBS) Minimum score: 7 Maximum score: 35 Higher scores indicate higher positive mental well-being (Better outcome).

次要结局

  • Depressive symptoms(8 weeks)
  • Anxiety symptoms(8 weeks)
  • Loneliness(8 weeks)

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Chua Yu Cong, Eugene

Family Physician, Consultant

National Healthcare Group Polyclinics

研究点 (1)

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