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Recruiting NCT07361159

Health and Wellness Coaching to Improve Thoracic Transplant Caregiver Self-Efficacy

No phase Interventional Wellbeing

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Health and Wellness Coaching.
Who it may be relevant to
Registry conditions: Wellbeing. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

This is a pilot study examining the effects of telephonic health and wellness coaching on self-efficacy and caregiving burden for caregivers of patients awaiting heart or lung transplant.

Interventions

  • Behavioral Health and Wellness Coaching
    Participants will receive health and wellness coaching. Coaching sessions will occur via telephone with a National Board-Certified Health and Wellness Coach (NBC-HWC). Sessions will be motivational interview based and will be up to 30 minutes in length. Participants can receive up to 8 coaching sessions within 10 weeks.

Primary outcome measures

  • Caregiver Burden Scale (CBS) [Time frame: Completed at baseline and at study completion; 10 weeks after enrollment]
  • Caregiver Self-Efficacy Scale [Time frame: Completed at baseline and at study completion; 10 weeks after enrollment]

Eligibility criteria

Inclusion criteria

  • Aged 18 years or older
  • Primary caregivers of patients listed (active, deferred, or temporarily inactive) for lung, heart/lung, or heart transplantation at Mayo Clinic in Rochester

Exclusion criteria

  • Individuals younger than 18 years old
  • Individuals who are non-English speaking, non-verbal, or extremely hard of hearing

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Supportive care

Study locations

United States · 1 center
  • Mayo Clinic — Rochester

Identifiers

NCT: NCT07361159 · 25-009890

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗