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Physical Therapy in Patients Undergoing Allo-HSCT With cGVHD

Physical Therapy in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation With a Diagnosis of Chronic Graft-versus-host Disease: A Randomized Clinical Trial.

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06279585
Enrollment
108
Registered
2024-02-28
Start date
2024-03-01
Completion date
2025-09-30
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Graft-versus-host-disease, Graft Versus Host Disease, Chronic, Hematological Malignancy, Hematologic Cancer, Stem Cell Transplant Complications

Keywords

Hematopoietic Stem Cell Transplantation, Graft versus host disease, Physiotherapy, Rehabilitation, Physical therapy, Exercise

Brief summary

Allogeneic Hematopoietic Stem Cell Transplantation (alloHSCT) represents the only curative option for many patients diagnosed with various hematologic neoplasms. Procedure-related morbidity and mortality pose challenges to long-term outcomes and quality of life, especially among patients who develop chronic graft-versus-host disease (cGVHD). There is a gap in healthcare that comprehensively addresses the specific needs of these patients. Physical therapy as an adjuvant treatment, through therapeutic exercise involving muscle strength and cardiorespiratory endurance, has shown positive influences on health markers and serves as a strong medical ally in similar profiles. Although these strategies could be reproducible and potentially beneficial for cGVHD patients, research has been limited to date, with the role of physical therapy possibly underutilized in this field. Justification: Unaddressed medical gap with no rigorously scientific responses specific to cGVHD. Objectives: This project aims to conduct the first randomized clinical trial from a physical therapy perspective as an adjuvant treatment for patients undergoing alloHSCT diagnosed with cGVHD.

Detailed description

Design: Prospective controlled clinical trial. Location: Virgen del Rocío University Hospital, Hematology Unit. Statistical analysis plan:The data will be analyzed using SPSS v.26 software for Windows and Epidat 4.2. All statistical tests will be conducted considering a 95% confidence interval (p-value \<0.05). To compare the score of the main outcome measure, quality of life (score range 0-200), between the experimental and control groups, the t-test or Mann-Whitney test will be employed (depending on the normality of the data). The comparison will be conducted at three time points (T0, T1, and T2). Furthermore, multivariate analysis will be performed using generalized equations of repeated measures to determine score changes between the groups. Since it is a Likert scale-based score, the Friedman test will be used to compare score changes, employing the Bonferroni test for pairwise comparisons.

Interventions

OTHERPhysical therapy

Health education sessions and combined therapeutic exercise sessions, based on muscular strength training and cardiorespiratory endurance.

Sponsors

University of Seville
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with chronic Graft-Versus-Host Disease (cGVHD) treated at Virgen del Rocío University Hospital will be invited to participate in the trial (n=108), under the following eligibility criteria: Inclusion criteria: * Adult (18 years or older); Underwent allogeneic hematopoietic stem cell transplantation (alloHSCT) diagnosed with cGVHD; No medical contraindication for moderate or high-intensity exercise; Proficiency in the Spanish language; Have access to the internet.

Exclusion criteria

* Unable to perform initial or final physical assessments; Having serious pre-existing conditions before the oncological diagnosis or diseases that are not or poorly controlled; Not signing or delivering the informed consent on the indicated date.

Design outcomes

Primary

MeasureTime frameDescription
Health-related quality of lifeWeek 1, Week 6, and Week 13MEASURE NAME: Functional Assessment of Cancer Therapy - Bone Marrow Transplantation (FACT-BMT); VERSION: 4; NUMBER OF ITEMS: 50; RESPONSE SCALE: 5 point Likert-type scale; SCORING:Manual scoring template, some items are reverse scored. Higher score represents better quality of life.
Chronic Graft-Versus-Host Disease (cGVHD) symptom burdenWeek 1, Week 6, and Week 13Modified Lee Chronic Graft-Versus-Host Disease Symptom Scale (mLSS) for 7 days. This is an instrument with 7 domains (skin, eyes, mouth, lungs, nutrition, energy, and psychiatry) and a total of 28 items to assess. The response options for Please inform us if any of the following problems have bothered you in the last 7 days range from 0 to 4 (Not at all, A little, Moderately, Quite a bit, Extremely). A difference of 5 to 6 points (standard deviation) will be considered clinically significant. Subscales range from 0 to 100, with a higher score indicating worse symptoms.

Secondary

MeasureTime frameDescription
Functional statusWeek 1, Week 6, and Week 13Human Activity Profile (HAP)
DistressWeek 1, Week 6, and Week 13Distress-Thermometer
MoodWeek 1, Week 6, and Week 13Mood Assessment Scale (MAS); Designed to assess transient mood states, both positive and negative, in any individual at any time, through 16 items divided into four scales (depression, anxiety, hostility, and joy), each defined by 4 items and evaluated using the Likert scale, with scores ranging from 0 to 10. The values for each category are calculated by the mean. All 16 statements have the same structure; they all begin with the phrase I feel and end with an adjective describing a mood state.
Muscular strengthWeek 1, Week 6, and Week 13Sit-to- Stand test y Handrig strength test
Biological markersWeek 1, Week 6, and Week 13Cytokines (interleukins) and lymphocytic populations as part of routine analysis. Blood sample.
Responses to medical treatmentWeek 1, Week 6, and Week 13NIH Criteria
AnxietyWeek 1, Week 6, and Week 13Hospital Anxiety and Depression Scale (HADS) questionnaire; The Hospital Anxiety and Depression Scale questionnaire (HADS); a useful tool for identifying anxiety and depression states in cancer patients and applicable during clinical practice. The two categories consist of one subscale each, with seven items rated from 0 to 4 points, with higher scores (in the range of 0 to 21) indicating anxious and depressive states. Participants should respond considering how they felt and/or behaved during the last seven days.
Cardiorespiratory fitnessWeek 1, Week 6, and Week 132-min Walk Test

Countries

Spain

Contacts

Primary ContactRaquel P Aguilar, PhDcand
raquelijorml@gmail.com955 013 260
Backup ContactJosé Antonio P Simón, PHD
josea.perez.simon.sspa@juntadeandalucia.es955 013 260

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026