Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
20

Summary

Conditions
Acute Myeloid Leukemia
Type
Interventional
Phase
Not Applicable
Design
Allocation: Non-RandomizedIntervention Model: Sequential AssignmentIntervention Model Description: This is a feasibility study. This study is conducted on one unit and to reduce bias and contamination, the control patients will be recruited and consented first. After recruitment of the 20 control patients, we will then recruit 20 intervention patients.Masking: None (Open Label)Primary Purpose: Supportive Care

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

The primary objective of the study is to assess feasibility, acceptability, and change in pre and post measures of symptoms, function, and QOL by administering the PACT intervention. The first ten participants in the control group will receive usual care. The next 10 participants will receive the PA...

The primary objective of the study is to assess feasibility, acceptability, and change in pre and post measures of symptoms, function, and QOL by administering the PACT intervention. The first ten participants in the control group will receive usual care. The next 10 participants will receive the PACT intervention. Each participant in the intervention group will be cared by a collaborative, multidisciplinary, integrated team including RNs, OTs and PTs.

Tracking Information

NCT #
NCT04570709
Collaborators
Not Provided
Investigators
Principal Investigator: Ashley Bryant, PhD, RN University of North Carolina, Chapel Hill