Hematopoietic Stem Cell Transplantation Empowerment Program

NCT07781046 | Completed DMC

• 1 other identifier: IRP.437
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this study is to evaluate the impact of an empowerment program for patients undergoing stem cell transplantation on their clinical outcomes. The research hypothesis are:

• Patients who participate in the proposed empowerment program will exhibit a significant improvement in their knowledge related to stem cell transplantation than those who don't.
• Patients who participate in the proposed empowerment program will exhibit a significant improvement in their self-care practices than those who don't.
• Patients who participate in the proposed empowerment program will exhibit a significant improvement in their health-related quality of life than those who don't. The study sample was divided into control and study groups. Study group (A) who was received routine care in addition to empowerment program, while control group (B) who was received routine care only.

Conditions

Stem Cell Transplantation, Hematopoietic

Keywords

Stem Cell Transplantation; Hematopoietic; Empowerment program

Outcome Measures

Primary Outcomes (1)

• Patient's demographic and health-relevant Data

  A structured interview questionnaire developed by the researcher will be used to collect patients' demographic and health-relevant characteristics. Demographic data will include age, sex, occupation, marital status, and educational level. Health-relevant data will include diagnosis, current and previous medical history, genetic diseases, source and type of stem cell transplantation, and family history of previous stem cell transplantation.

  Baseline (pre-intervention)

Secondary Outcomes (1)

• Patient's Knowledge Assessment Questionnaire

  Baseline, immediately post-intervention, and 3 months post-intervention

Other Outcomes (1)

• Patient's Self-Care Practices Observational Checklist

  Baseline, immediately post-intervention, and 3 months post-intervention

Study Arms (1)

Control and study groups

EXPERIMENTAL

The study sample was divided into control and study groups. Study group (A) who was received routine care in addition to empowerment program, while control group (B) who was received routine care only.

Behavioral: Empowerment program

Interventions

Empowerment program BEHAVIORAL

A structured nursing-led empowerment program designed to improve patients' knowledge, self-care skills, and quality of life.

Control and study groups

Eligibility Criteria

• Age: 21 Years - 60 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Conscious, adult patients at the age of 20-60 years from both genders.
• Able to communicate verbally and exhibited a willingness to participate in the study.

You may not qualify if:

• Patients with physical or mental limitations.
• Patients involved in other programs.

Sponsors & Collaborators

• Mansoura University: lead

Study Sites (1)

Faculty of Nursing

Al Mansurah, Dakhlia, 35516, Egypt

Location

Study Officials

• Ola Ebrahim Elsherbiny, Assistant professor

  Faculty of Nursing, Mansoura University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Assistant Professor of Medical Surgical Nursing, Faculty of Nursing, Mansoura University

Model Details: a quasi-experimental, two-group pretest-posttest design

Study Record Dates

• First Submitted: August 17, 2026
• First Posted: August 24, 2026
• Study Start: January 1, 2025
• Primary Completion: February 1, 2026
• Study Completion: February 1, 2026
• Last Updated: August 24, 2026

Record last verified: 2026-08

Data Sharing

• IPD Sharing: Will not share

Locations

EG (1)