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临床试验/NCT06883838
NCT06883838Enrolling By Invitation不适用

Enhancing Primary Care Capacity for Cancer Survivorship Care Delivery in Community Health Clinics

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 5,584 人开始时间: 2025年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
5,584
试验地点
2
主要终点
Proportion of eligible cancer survivors screened for second primary cancers

研究概览

简要总结

The purpose of this study is to implement a clinic-level cancer survivorship care delivery intervention in partnership with community health center clinicians, patients, and community representatives to test effectiveness of the intervention to improve patient and clinician outcomes and to evaluate implementation of the intervention using an iterative, concurrent mixed-methods approach guided by the Practice Change Model.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • •(participants):
  • •at least one visit to the Community Health Centers (CHCs) in the prior year

排除标准

  • •(participants):
  • •- no history of cancer recorded in the problem list or past medical history in the medical record
  • •Inclusion Criteria (clinicians):
  • •employed clinicians (e.g. physicians, nurses, pharmacists, or other allied health professionals) and non-clinician staff of the participating CHC clinics

研究组 & 干预措施

Step 4 (2 clinics)- 24 months control then 12 months intervention

Experimental

干预措施: Survivorship care delivery intervention (Behavioral)

Step 1 (2 clinics)-6 months control then 12 months intervention

Experimental

干预措施: Survivorship care delivery intervention (Behavioral)

Step 2 (2 clinics)-12 months control then 12 months intervention

Experimental

干预措施: Survivorship care delivery intervention (Behavioral)

Step 3 (2 clinics)-18 months control then 12 months intervention

Experimental

干预措施: Survivorship care delivery intervention (Behavioral)

结局指标

主要结局

Proportion of eligible cancer survivors screened for second primary cancers

时间窗: every 6 months from baseline to end of study (about 36 months from baseline)

Data derived from electronic health records

次要结局

  • Change in proportion of primary care clinician knowledge of cancer survivorship care(baseline, six months following end of intervention period)
  • Change proportion of survivors that report better experience of provider communication as assessed by the adapted Consumer Assessment of Healthcare Providers and Systems (CAHPS 4.0)(baseline, six months following end of intervention period)
  • Change proportion of survivors that report better experience of care coordination as assessed by the adapted Consumer Assessment of Healthcare Providers and Systems (CAHPS 4.0)(baseline, six months following end of intervention period)
  • Proportion of survivors who received guideline-recommended surveillance for the most prevalent cancers (breast colorectal, prostate, cervical, and lung)(every 6 months from baseline to end of study (about 36 months from baseline))

研究者

发起方
The University of Texas Health Science Center, Houston
申办方类型
Other
责任方
Principal Investigator
主要研究者

Bijal.A.Balasubramanian

Professor

The University of Texas Health Science Center, Houston

研究点 (2)

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