NCT07066592

Brief Summary

Aim of the Study: The aim of this study is to examine the effect of prehabilitation education delivered via a mobile-compatible website on the quality of life and symptom evaluation of patients undergoing hematopoietic stem cell transplantation (HSCT). Research Questions: What is the effect of prehabilitation education delivered via a mobile-compatible website on the quality of life of stem cell transplant patients? What is the effect of prehabilitation education delivered via a mobile-compatible website on the symptom management of stem cell transplant patients? Method: In this study, patients will be randomly assigned to one of two groups: One group will receive prehabilitation education through a mobile-compatible website. The other group will receive standard educational procedures.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 13, 2024

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

June 25, 2025

Completed
20 days until next milestone

First Posted

Study publicly available on registry

July 15, 2025

Completed
16 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2025

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 15, 2025

Completed
Last Updated

July 15, 2025

Status Verified

December 1, 2024

Enrollment Period

8 months

First QC Date

June 25, 2025

Last Update Submit

July 4, 2025

Conditions

Keywords

prehabilitationquality of lifebone marrow transplantationeducation

Outcome Measures

Primary Outcomes (2)

  • symptom management

    Edmonton Symptom Assessment Scale. Each symptom is evaluated using numerical ratings ranging from 0 to 10. A score of 0 indicates that the symptom is absent, while a score of 10 indicates that the symptom is felt very severely. The severity of the symptom increases progressively from 0 to 10. (The changes will be evaluated from the baseline level to the day of transplantation and up to the day of discharge. This period takes approximately 3-4 weeks on average)

    The baseline and average 3-4 weeks

  • quality of functionality

    Functional Assessment of Cancer Therapy-Bone Marrow Transplant (4th version) The minimum score obtainable from the FACT-BMT scale is 0, and the maximum score is 148. Higher scores indicate a better quality of life. (The changes will be evaluated from the baseline level to the day of transplantation and up to the day of discharge. This period takes approximately 3-4 weeks on average)

    The baseline and average 3-4 weeks

Study Arms (2)

Prehabilitation education provided via mobile compatible website

EXPERIMENTAL

Participants will receive access to the educational website containing information on the stem cell transplantation process, consisting of 9 sections, one week prior to hospital admission.

Behavioral: Prehabilitation education provided via mobile compatible website

Control

NO INTERVENTION

Participants will receive routine care.

Interventions

The prehabilitation education delivered through a mobile-compatible website was developed specifically for patients who are candidates for stem cell transplantation. Through this platform, patients can easily and quickly access accurate information on managing potential symptoms during the transplant process, as well as guidance on nutrition and exercise aimed at improving their quality of life.

Prehabilitation education provided via mobile compatible website

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Undergoing Hematopoietic Stem Cell Transplantation (HSCT) for the first time
  • Having no musculoskeletal problems that would prevent physical activity
  • Volunteering to participate in the study
  • Between 18 and 70 years of age
  • Having access to and the ability to use a mobile phone and the internet
  • Literate in Turkish (able to read and write in Turkish)

You may not qualify if:

  • Having a condition that prevents effective communication
  • Being illiterate (unable to read and write)
  • Inability to use technology

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Oncology Training and Research Hospital

Ankara, Turkey (Türkiye)

Location

Related Publications (3)

  • Normann AJ, Mo CC, Wilson RL, Perez M, Cutler C, Uno H, Thompson LV, Skinner TL, Richardson PG, Marinac CR, Dieli-Conwright CM. Prehabilitation Exercise Training to Target Improved Muscle Strength in Pretransplant Patients Diagnosed With Multiple Myeloma: Protocol for a Pilot Randomized Controlled Trial. JMIR Res Protoc. 2024 Dec 19;13:e64905. doi: 10.2196/64905.

    PMID: 39701583BACKGROUND
  • Naumann K, Singh B, Bushaway S, Crane R, Deepak S, Hartland A, Konstantopoulos P, Mansell E, Marinelli V, Pallotta V, Tolfts A, Virieux A, Wall M, Wilksch S, Zhuang M, Atkinson M, Maher C. Investigating the impact of multidisciplinary prehabilitation on deconditioning in patients eligible for haematopoietic allogenic stem cell transplantation: protocol for a feasibility trial. BMJ Open. 2024 Sep 5;14(9):e084372. doi: 10.1136/bmjopen-2024-084372.

    PMID: 39237275BACKGROUND
  • Dennett AM, Porter J, Ting SB, Taylor NF. Prehabilitation to improve function after autologous stem cell transplantation: A pilot randomized controlled trial (PIRATE). Support Care Cancer. 2025 Feb 7;33(3):164. doi: 10.1007/s00520-025-09179-1.

    PMID: 39920425BACKGROUND

MeSH Terms

Conditions

Hematologic Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsHematologic DiseasesHemic and Lymphatic Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 25, 2025

First Posted

July 15, 2025

Study Start

December 13, 2024

Primary Completion

July 31, 2025

Study Completion

August 15, 2025

Last Updated

July 15, 2025

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will not share

Locations