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Recruiting NCT04115241

Activity Levels in Bone Marrow Transplant Patients

Observational Bone Marrow Transplant

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Actigraph, Grip strength test.
Who it may be relevant to
Registry conditions: Bone Marrow Transplant. Basic parameters: 18 years — 99 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Participants in this study will be receiving a bone marrow transplant. This study is designed to evaluate correlations between activity levels and length of stay, quality of life, and hand grip strength.

Detailed description

Participants in this study will be receiving a bone marrow transplant. Participants will be given actigraphs to wear around their waists starting 3 weeks prior to bone marrow transplants until they are discharged from the hospital. Participants will be asked to complete quality of life questionnaires and hand grip tests at three separate time points during their hospitalizations. All data gathered from these activities will be compared with patients' activity levels gathered from the actigraphs both before and during the hospitalization. This study is designed to determine the relationship between activity levels and length of stay, quality of life, and hand grip strength.

Interventions

  • Device Actigraph
    Actigraphs are non-invasive, wearable devices that measure activity levels using an accelerometer
  • Other Grip strength test
    The purpose of this test is to measure the maximum isometric strength of the hand and forearm muscles

Primary outcome measures

  • To determine the correlation between activity levels and length of stay in hospital [Time frame: From study intitiation for up to 5 years]
  • To determine the correlation between activity levels and quality of life [Time frame: From study intitiation for up to 5 years]
  • To determine the correlation between activity levels and hand grip strength [Time frame: From study intitiation for up to 5 years]
Secondary outcome measures (1)
  • To determine barriers to activity for patients recovering from bone marrow transplantation and design an intervention to increase activity levels in patients post-transplantation [Time frame: From study intitiation for up to 5 years]

Eligibility criteria

Patients who will be receiving a bone marrow transplant are eligible for this study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

United States · 1 center
  • University of Iowa — Iowa City

Identifiers

NCT: NCT04115241 · 202208637-B

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗