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Clinical Trials/NCT04639700
NCT04639700
Withdrawn
N/A

A Pilot Study to Evaluate the Feasibility of an Intervention for Caregivers of Patients Who Have Recently Undergone HSCT

Overview

Phase
N/A
Intervention
Not specified
Conditions
Caregiver Anxiety
Sponsor
Case Comprehensive Cancer Center
Primary Endpoint
Mean caregiver satisfaction scores
Status
Withdrawn
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to find out if providing support to caregivers of patients who have recently had a HSCT is possible and helpful.

Detailed Description

This study will test the feasibility, acceptability, usability, satisfaction and preliminary efficacy of a behavioral (psychoeducation) intervention. All participants will receive the standard post-hospital HSCT information for patient follow-up care as provided by the patient's oncologist. In addition, the all participants will receive 4 individual sessions with an interventionist.

Registry
clinicaltrials.gov
Start Date
June 2021
End Date
November 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • An adult family or friend of a patient who has been discharged from the hospital in the past 1-2 weeks after receiving HSCT
  • Identifies himself/herself as the caregiver who will be responsible for the patient's care post-HSCT
  • Has English as their primary language

Exclusion Criteria

  • Not meeting inclusion criteria

Outcomes

Primary Outcomes

Mean caregiver satisfaction scores

Time Frame: At the end of each intervention session and end of study evaluation, up to 2 months

Caregiver Satisfaction scores as measured by Likert Scale. After completing each module, they will be sent via REDCap a single item evaluation scale (0 -10; 0=Not at all satisfied; 10=Highly satisfied). Scores \>7 will be considered acceptable. Mean and standard deviation will be reported.

Percent of enrollment of eligible participants

Time Frame: At 2 months

Feasibility as measured by percent of enrollment of eligible participants

Percent of participants completing intervention

Time Frame: At 2 months

Feasibility as measured by intervention completion

Acceptability Scale scores

Time Frame: At 2 months

Caregiver Acceptability as measured by Acceptability Scale scores. Overall score ranging from 6-30. According to prior research, a score of 80% of higher (total score of 24 or higher) is considered acceptable for use.

Retention rate

Time Frame: At 2 months

Feasibility as measured by percent of participants retained in full study (aim: 90% retention at the end of the 2-month intervention)

Data collection completion rate

Time Frame: At 2 months

Feasibility as measured by completion of data collection across study timepoints

System Usability Scale scores

Time Frame: At 2 months

Caregiver Usability as measured by the System Usability Scale. This is a 10 item scale scored on a 5 point Likert scale with total summed scores ranging from 0-50. Total scores are multiplied by 2 to produce an overall score ranging from 0-100 with scores \> 68 considered to be above average usability

Average time to recruit dyads in months

Time Frame: At 2 months

Feasibility as measured by time to identify and recruit dyads in months (benchmark 3 months)

Secondary Outcomes

  • NCCN Distress Thermometer scores(At baseline and at 2 months)
  • PROMISR Short Form v1.0 - Anxiety(At baseline and at 2 months)
  • PROMISRv.1.2 - GlobalHealth scores(At baseline and at 2 months)

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