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Physical Activity in Children During Hematopoietic Stem Cells Transplantation (HSCT)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03842735
Recruitment Status : Completed
First Posted : February 15, 2019
Last Update Posted : March 22, 2021
Sponsor:
Information provided by (Responsible Party):
Francesca Rossi, Azienda Ospedaliera Città della Salute e della Scienza di Torino

Brief Summary:
This interventional study was designed to assess the validity and the impact of a rehabilitation program on pediatric cancer patients undergoing hematopoietic stem cells transplantation (HSCT). Each participant will be randomly assigned to either an experimental or control (counseling rehabilitation care) group. The experimental group participate in an inpatient rehabilitation program for the duration of HSCT pathway. The program include standardized activities for 5 days a week in the child's room or in a pediatric gym at the hospital.

Condition or disease Intervention/treatment Phase
Hematopoietic Stem Cell Transplantation Child Adolescent Other: exercise and rehabilitation counselling Behavioral: rehabilitation counselling Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 80 participants
Allocation: Non-Randomized
Intervention Model: Crossover Assignment
Intervention Model Description: Eligible patients who provided consent were assigned to one of the two groups according to a "cluster time" selection model. The methodology was discussed and agreed with expert methodologists of the A.O.U. Città della Salute e della Scienza research group and based assignation to the two groups according to the time of hospitalization: EG enrollment May 2016-December 2016, March 2017-May 2017, November 2017-June 2018 and CG enrollment January 2017-February 2017, June 2017-October 2017, July 2018-August 2018.
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: Promotion of Physical Activity for Children and Adolescents Undergoing Hematopoietic Stem Cells Transplantation (HSCT) During the In-patient Phase
Actual Study Start Date : May 23, 2016
Actual Primary Completion Date : December 31, 2019
Actual Study Completion Date : February 28, 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Rehabilitation

Arm Intervention/treatment
Experimental: exercise and rehabilitation counselling
Subjects enrolled in exercise group make physical exercises and receive rehabilitative counselling indications
Other: exercise and rehabilitation counselling
The intervention consists in a standardized physical exercise (PE) and rehabilitation counselling indications (RCI). PE is done 5 days/week (2 days in autonomy by the patient with parents support and 3 days supervised). Each session lasts 30 minutes and this is supervised by one therapist for all patients. Patients are enrolled in an EP composed by three different types of exercises, each carried out for 10 minutes per session: muscle strength exercises for upper and lower extremities preceded by warming up, aerobic exercises and stretching. The kind of exercise is differentiated by age range (children, 5-12 years and adolescents, 13-18 years).
Other Name: rehabilitation

Behavioral: rehabilitation counselling
RCI, which have to be followed daily, consist in some practical advice was given on how to adopt an active lifestyle during the recovery (e.g., getting up to go to the bathroom, getting up to move to the window to talk with visitors, sit on chair to have school lessons).

rehabilitation counselling
Subjects enrolled in exercise group only receive rehabilitative counseling indications.
Behavioral: rehabilitation counselling
RCI, which have to be followed daily, consist in some practical advice was given on how to adopt an active lifestyle during the recovery (e.g., getting up to go to the bathroom, getting up to move to the window to talk with visitors, sit on chair to have school lessons).




Primary Outcome Measures :
  1. change in global motor skills level [ Time Frame: this outcome it is measured in the week before HSCT [Time 0] and post hematopoietic stem cells transplantation (HSCT), after the discharge from stem cells unit (SCU), at an average of 40 days after Time 0 [Time 1] ]
    The Gross Motor Function Measure (GMFM), version -88 for children who aged between 0-4 years, and version-Acute Lymphoblastic Leukemia (ALL) for older subjects. The GMFM-88 is composed by 88 items, while the GMFM-ALL is composed by 21 items. Each item can be scored as 0, 1, 2, 3, or "not tested". Scoring key: 0 - does not initiate, 1 - initiates, 2 - partially completes, and 3 - completed. The total score for GMFM-88 can be between 0 and 264, while for the GMFM-ALL can vary from 0 to 63.

  2. change in range of passive ankle dorsiflexion [ Time Frame: this outcome it is measured in the week before HSCT [Time 0] and post HSCT, after the discharge from SCU, at an average of 40 days after Time 0 [Time 1] ]
    Goniometer

  3. rate of immune cells recovery [ Time Frame: this outcome it is measured 35 days after the first day of infusion ("day zero") ]
    blood counts of leukocytes, monocytes, and lymphocytes and main lymphocyte subpopulations and dendritic cells

  4. participation rate at the exercise program [ Time Frame: 24 hours ]
    Parents are required to record in appropriate grids their child's daily activities and adolescents fill them in themselves. The therapist goes 3 times/week to check that the diary is filled in correctly. This outcome it is measured daily during the stay in the SCU.

  5. adhesion rate to rehabilitative counselling indications [ Time Frame: 24 hours ]
    Parents are required to record in appropriate grids their child's daily activities and adolescents fill them in themselves. The therapist goes 3 times/week to check that the diary is filled in correctly. This outcome it is measured daily during the stay in the SCU.


Secondary Outcome Measures :
  1. change in functional motility level [ Time Frame: this outcome it is measured in the week before HSCT [Time 0] and post HSCT, after the discharge from SCU, at an average of 40 days after Time 0 [Time 1] ]
    Time Up and Go Test (TUG); it is measured only in children who aged more than 5 years.

  2. change in tibialis anterior and quadriceps muscles strength level [ Time Frame: this outcome it is measured in the week before HSCT [Time 0] and post HSCT, after the discharge from SCU, at an average of 40 days after Time 0 [Time 1] ]

    Medical Research Council Scale (MRC). This method involves testing key muscles from the upper and lower extremities against the examiner's resistance and grading the patient's strength on a 0 to 5 scale accordingly:

    0 No muscle activation

    1. Trace muscle activation, such as a twitch, without achieving full range of motion
    2. Muscle activation with gravity eliminated, achieving full range of motion
    3. Muscle activation against gravity, full range of motion
    4. Muscle activation against some resistance, full range of motion
    5. Muscle activation against examiner's full resistance, full range of motion It is measured only in children who aged more than 5 years.

  3. change in flexibility level of the lower back and hamstring muscles [ Time Frame: this outcome it is measured in the week before HSCT [Time 0] and post HSCT, after the discharge from SCU, at an average of 40 days after Time 0 [Time 1] ]
    Seat and Reach Test; it is measured only in children who aged more than 5 years.

  4. change in functional exercise capacity level [ Time Frame: this outcome it is measured in the week before HSCT [Time 0] and post HSCT, after the discharge from SCU, at an average of 40 days after Time 0 [Time 1] ]
    Two Minute Walk Test; it is measured only in children who aged more than 5 years.

  5. change in fatigue level [ Time Frame: this outcome it is measured in the week before HSCT [Time 0] and post HSCT, after the discharge from SCU, at an average of 40 days after Time 0 [Time 1] ]

    PedsQL Multidimensional Fatigue Scale. The PedsQL is an interview where item Scaling is based on 5-point Likert scale from 0 (Never) to 4 (Almost always).Items are reversed scored and linearly transformed to a 0-100 scale as follows:

    0=100, 1=75, 2=50, 3=25, 4=0. Total Score: Sum of all the items over the number of items answered.


  6. change of quality of life level: PedsQL Cancer Module [ Time Frame: this outcome it is measured in the week before HSCT [Time 0] and post HSCT, after the discharge from SCU, at an average of 40 days after Time 0 [Time 1] ]
    PedsQL Cancer Module



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Ages Eligible for Study:   6 Months to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • i) being children or adolescents (6 months -18 years old);
  • ii) to have a diagnosis of oncological or hematological disease;
  • iii) receiving an autologous or allogeneic HSCT;
  • iv) to have spoken and written Italian language comprehension, both by children/adolescents and by parents.

Exclusion Criteria:

  • i) to be affected by cognitive difficulties that preclude to the program's participation;
  • ii) to be already undergoing rehabilitation before the entrance in the Transplantation Stem Cell Unit (TSCU).

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03842735


Locations
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Italy
A.O.U. Città della Salute e della Scienza - Regina Margherita children hospital
Turin, Italy, 10126
Sponsors and Collaborators
Azienda Ospedaliera Città della Salute e della Scienza di Torino
Investigators
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Principal Investigator: Francesca Rossi, Dr A.O.U. Città della Salute e della Scienza - OIRM, Turin, Italy
Publications:

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Responsible Party: Francesca Rossi, Development Neuro and Psychomotor Therapist, Azienda Ospedaliera Città della Salute e della Scienza di Torino
ClinicalTrials.gov Identifier: NCT03842735    
Other Study ID Numbers: PHYSICALACTIVITYHSCT0-18YSIPP
First Posted: February 15, 2019    Key Record Dates
Last Update Posted: March 22, 2021
Last Verified: March 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Francesca Rossi, Azienda Ospedaliera Città della Salute e della Scienza di Torino:
Physiotherapy
Rehabilitation
Exercise