跳至主要内容
临床试验/NCT07116018
NCT07116018招募中不适用

Feasibility Testing of an Adapted Psychoeducational Intervention for Caregivers of Patients Undergoing Allogeneic Stem Cell Transplant for Hematological Malignancy

University Health Network, Toronto2 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2025年5月21日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
22
试验地点
2
主要终点
Feasibility of Intervention Measure (FIM)

研究概览

简要总结

Background: Caregivers of patients undergoing allogeneic hematopoietic cell transplantation (alloHCT) for hematological malignancies face significant challenges that can impact their well-being. This study aims to evaluate the feasibility and acceptability of an adapted psychoeducational intervention(PEI) designed to support these caregivers.

Methods: This study will recruit caregivers of alloHCT patients. Participants will be enrolled during pre-transplant clinic visits, typically 2-4 weeks before the scheduled transplant. The intervention consists of eight sessions over 12 weeks, delivered via Microsoft Teams by a nurse facilitator. In the adapted PEI, participants will learn stress management, coping strategies, energy management, goal-setting, communication skills, and support resource access through interactive exercises. Data Collection: Participants will complete questionnaires at three time points: pre-intervention, one month post-transplant, and three months post-transplant. The final assessment will include additional questions about feasibility, acceptability and the initial efficacy of the adapted PEI.

Outcomes: The primary outcomes will be the feasibility and acceptability of the adapted psychoeducational intervention (PEI). Secondary outcomes will include initial efficacy of the adapted PEI on caregiver outcomes such as depression, anxiety, satisfaction with caregiving and quality of life.

Significance: This research aims to assess the feasibility, acceptability and initial efficacy of implementing the adapted PEI for alloHCT caregivers. If found feasible and acceptable, this intervention could potentially improve caregivers' ability to manage caregiving stressors and pave the way for larger-scale randomized studies and implementation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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

入选标准

  • Must be caregiver for an adult patient diagnosed with hematological malignancy who is scheduled to receive allogeneic stem cell transplant.
  • Are recruited and consented to participate in the caregiver study during the patient's pre-transplant screening phase for allogeneic stem cell transplant.
  • Will provide care for the patient from the day of allogeneic stem cell transplant up to 100 days post- transplant.
  • Are willing to begin the study intervention no earlier than 0-day post-transplant and not later than 2-weeks post-transplant.

排除标准

  • Less than 18 years of age
  • Non-English speaking

结局指标

主要结局

Feasibility of Intervention Measure (FIM)

时间窗: 3 months

The Feasibility of Intervention Measure (FIM) revised to evaluated the psychoeducation program comprises 4-items regarding the respondent's perceptions of the feasibility of the intervention. Responses range from 1 (completely disagree) to 5 (completely agree). Scale value is computed by averaging responses and ranges from 1-5. Higher values indicate greater feasibility of the intervention.

Intervention Appropriateness Measure (IAM)

时间窗: 3 months

The Intervention Appropriate Measure (IAM) revised to evaluated the psychoeducation program comprises 4-items regarding the respondent's perceptions of the appropriateness of the intervention. Responses range from 1 (completely disagree) to 5 (completely agree). Scale value is computed by averaging responses and ranges from 1-5. Higher values indicate greater appropriateness of the intervention.

Acceptability of Intervention Measure (AIM)

时间窗: 3 months

The Acceptability of Intervention Measure (AIM) revised to evaluated the psychoeducation program comprises 4-items regarding the respondent's perceptions of the acceptability of the intervention. Responses range from 1 (completely disagree) to 5 (completely agree). Scale value is computed by averaging responses and ranges from 1-5. Higher values indicate greater acceptability of the intervention.

次要结局

  • Perceived Stress(Baseline, 1 month, 3 months)
  • Depression(Baseline, 1 month, 3 months)
  • Caregiver Quality of Life(Baseline, 1 month, 3 months)
  • Satisfaction with Life(Baseline, 1 month, 3 months)
  • Anxiety(Baseline, 1 month, 3 months)

研究者

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

Samantha Mayo

Clinician Investigator

University Health Network, Toronto

研究点 (2)

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