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Resiliency in Older Adults Undergoing Bone Marrow Transplant (REBOUND)

Primary Purpose

Leukemia, Lymphoma, Blood Cancer

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bone Marrow Transplant (BMT)
Sponsored by
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Leukemia focused on measuring Allogeneic blood and marrow transplantation (alloBMT), Resiliency, REBOUND, over age 60

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Undergoing allogeneic bone marrow transplant at Johns Hopkins Hospital, the indication for which is a hematologic malignancy
  • Age ≥60 years
  • Ability to walk without human assistance
  • Enrollment in concomitant clinical research is permitted but not required
  • English-speaking
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

  • Unwillingness or inability to return at 6 months after transplantation for repeated evaluation
  • Non-English-speaking

Sites / Locations

  • Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Interventional Arm- Bone Marrow Transplant

Arm Description

Study visits will include the performance of assessments prior to the start of conditioning chemotherapy and at 1 month and 6 months post-BMT. Assessments include: Physical function assessments questionnaires about general health and current health compared to health one year ago assessments that measure cognition, attention and memory assessments regarding personality and psychological and social stressors Physiological measures including blood tests- 160 mL of blood during evaluations, and 90mL of blood at the day 180 visit. bone marrow aspirate collected during standard of care bone marrow biopsies pre-transplant and at day 180 Saliva collections pre-transplant ACTH Stimulation Test Oral Glucose Tolerance Test Holter Monitor- to record hear rate variability MRI pre-transplant and at Day 180 in a subset of 10 subjects

Outcomes

Primary Outcome Measures

Change in Physical Performance as assessed by Short Physical Performance Battery (SPPB)
5 measured criteria: unintentional weight loss, exhaustion, low energy expenditure, low grip strength, and slowed waking speed. Scores of 3, 4 and 5 are consistent with frailty, scores of 1 and 2 are consistent with pre-frailty status, and a score of 0 is consistent with a robust or resilient status.
Change in ability to perform activities of daily living as assessed by Instrumental Activities of Daily Living questionnaire
questions about ability to perform activities of daily living (IADL). Scored low functioning (0) to high functioning (8).
Change in upper extremity function as assessed by accelerometry
device worn on wrist for a 24hr period that measures physical activity and sedentary activity. Higher scores= more active.
Change in catecholamines levels as assessed in overnight urine collection samples
Changes in catecholamines level will be assessed in overnight urine collection samples. Levels fluctuate. Analysis will use the Johns Hopkins University (JHU) normal reference range for an adult is Metanephrine (normotensive):45-290 μg/24 hours. Metanephrine (hypertensive): 35-460 μg/24 hours .
Change in Frailty as assessed by the Frailty Phenotype instrument
Frailty Phenotype instrument is used to measure participants' walking speed and grip strength, includes questions about exhaustion, physical activity, weight loss. Higher scores indicate better functional state.
Change in Pittsburgh Fatigability Scale for Older Adults score
self-report tool that normalizes activities in terms of intensity and duration (PFS) this has a range of 0-50 with higher scores indicating greater physical fatigability.
Change in Borg Rating of Perceived Exertion Scale score
scale will be used immediately after a slow-paced 5-minute treadmill walk to assess fatigability (RPE). Higher score indicates higher perceived exertion.
Change in medical history and diseases/conditions self reporting
Questionnaire of past medical history as reported by a subject. This questionnaire does not have a score.
Change in health behaviors as assessed by a questionnaire
This assessment is of self determined overall health as reported by a participant, it has no score.
Change in reporting of patients traumas as assessed by the Hospitalizations, Surgeries, and Falls Questionnaire
Questionnaire includes items on hospitalizations, surgeries, and falls. it has no score.
Change in pain reporting as assessed by the Pain Assessment Questionnaire
questions on overall bodily pain intensity/frequency and pain-related function/interference. Higher scores equal more pain.
Change in anxiety reporting as assessed by the anxiety questionnaire
Questions to assess the presence and severity of anxiety; higher scores = more anxiety.
Change in trauma reporting as assessed by the trauma questionnaire
Questions to assess a participants reporting of any past experiences of several kinds of trauma. It has no score.
Change in cognitive function as assessed by Modified Mini-Mental State Examination
measure of global cognitive function (range 0-100). A score of 100 represents total cognitive function according to 3MS.
Change in cognitive ability as assessed by the Montreal Cognitive Assessment
measures global cognitive function (MoCA). Scores range between 0 and 30. A score of 26 or over is considered to be normal.
Change in cognitive function as assessed by the Digit Symbol Substitution Test (DSST)
participant fill in a series of symbols correctly coded within 90 seconds. The higher the score, the better the participant's performance.
Change in ability to cope with life challenges as assessed by the Coping Self-Efficacy Scale
11-point Likert scale measures perceived ability to cope effectively with life. Scale is 0-10 with 10 = best ability to cope and 0 = no ability to cope.
Change in sense of well-being as assessed by the Subscale of Ryff Psychological Well-being Scale
7-item Likert type scale (from strongly disagree to strongly agree) measures sense of direction and perception of purpose. Scale is 0-7 with 7 = best sense of well-being and 0 = no sense of well-being.
Change in perception and satisfaction with life as assessed by the Meaning in Life Questionnaire and Scale
Likert-type scale measuring perception of meaning and satisfaction with life (MLQ) Scale is 0-7 with 7 = best sense that life has meaning and 0 = no sense that life has meaning.
Change in personality as measured by the Ten Item Personality Inventory (TIPI) Scale
7 point Likert-type scale of disagree to agree with various aspects of personality measuring: extraversion, agreeableness, neuroticism, openness, conscientiousness. TIPI scale scoring. Extraversion: 1, 6R; Agreeableness: 2R, 7; Conscientiousness; 3, 8R; Emotional Stability: 4R, 9; Openness to Experiences: 5, 10R. ("R" denotes reverse-scored items)
Change in optimism as assessed by the Life Orientation Scale-Revised
5 point Likert scale, assessing optimism. 0= strongly disagree; 4 = strongly agree. The total score is from 0 to 24; higher scores indicate more optimism.
Change in perceived loneliness as assessed by the Loneliness Scale
Revised University of California, Los Angeles (UCLA) Loneliness Scale. Each question is rated on a 4-point scale: 1 = never; 2 = Rarely; 3 = Sometimes 4 = Always. All items are summed to give a total score. Higher scores indicate more loneliness
Change in perceived socio-economic status as assessed by the US socioeconomic questionnaire
10-rung ladder to assess a participant's perception of participant's status in society. To score this measure, researchers simply note the number of the rung (1-10) on which the respondent placed their "X".
Change in perceived financial strain as assessed by Financial Strain questionnaire
2 item measure evaluating difficulty and anxiety about money. Higher scores equal higher financial strain.
Change in feeling of community inclusion as assessed by the Social Cohesion Questionnaire
Participants rate their community by rate of agreement. Response is Agree a lot, a little, do not agree with 3 statements about their community.
Change in feeling of isolation as assessed by the Social Isolation/Engagement Questionnaire
7-item measure evaluating social isolation, participation and engagement with others. Higher scores= greater sense of isolation.
Change in perceived confidence in spirituality as assessed by the Religion/Spirituality Questionnaire
5-Item measure for use in epidemiological studies regarding spirituality. Score range from 5-27, with higher scores = more sense of spirituality
Change in feelings of depression as assessed by the Patient Health Questionnaire
Measures depressive symptoms in the last 2 weeks (PHQ-8)
Change in perceived childhood trauma as assessed by the Adverse Childhood Events (ACE) Scale
10-item measure to assess childhood abuse and household dysfunction. Response is yes/no. The ACE Scale is scored by summing the number of items for which respondents answered "yes."
Changes in perceived stress as assessed by the Perceived Stress Scale
5-point Likert scale measures the cognitive appraisal and perceptions of stress in life. Higher score= high level of perceived stress.
Change in bone marrow cell ratios as assessed by Bone Marrow Aspirate
aspirate will be collected during standard of care bone marrow biopsies and analyzed using JHU normal reference ranges.
Change in hemoglobin tests.
160 mL of blood during evaluations, and 90mL of blood at the day 180 visit. Assessment will be documents using Hopkins normal reference ranges
changes in salivary plasma free cortisol collection
Saliva collected at home by participants at 4 time points during a single 24 hour period. The mean salivary cortisol concentration is 15.5 +/- 0.8 nmol/L (range, 10.2-27.3) at 0800 h and 3.9 +/- 0.2 nmol/L (range, 2.2-4.1) at 2000 h.
Change in cortisol level
This is part of the ACTH Stimulation test to assess the reactivity of hypothalamic-pituitary-adrenal (HPA) axis. Test After the baseline blood draw is taken, 1mcg (low dose) Cosyntropin (synthetic ACTH) will be given intravenously by a research nursing staff followed by serial blood sampling to test for cortisol levels (mcg/dL).
Changes in interleukin (IL)-6 level
This is part of the ACTH Stimulation test to assess the reactivity of HPA axis. After the baseline blood draw is taken, 1mcg (low dose) Cosyntropin (synthetic ACTH) will be given intravenously by a research nursing staff followed by serial blood sampling to test for IL-6 levels (pg/ml).
Change in dehydroepiandrosterone (DHEA) level
This is part of the ACTH Stimulation test to assess the reactivity of HPA axis. After the baseline blood draw is taken, 1mcg (low dose) Cosyntropin (synthetic ACTH) will be given intravenously by a research nursing staff followed by serial blood sampling to test for DHEA levels (µg/dL).
Change in glucose tolerance as assessed by the Oral Glucose Tolerance Test (OGTT)
Participants will fast overnight and then be given the 75 gram glucose oral load followed by blood draws at 0, 30. 60 and 120 minutes. At 120min, below 140mg/dL= normal blood sugar. 200mg/dL or higher= diabetes
Change in heart rate variability as assessed by the "myPatch" Holter monitor
lightweight digital device that records and stores electrocardiogram (ECG) data on a continuous basis during study visits. A normal resting heart rate for adults ranges from 60 to 100 beats per minute. Generally, a lower heart rate at rest implies more efficient heart function.
Change in attention as assessed by the Flanker Inhibitory Control and Attention Test score
Measures attention and inhibitory control. Scoring is 0-10. Details and interpretations are available in the NIH toolbox scoring and interpretation guide.

Secondary Outcome Measures

Full Information

First Posted
November 26, 2019
Last Updated
February 22, 2023
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Collaborators
National Institutes of Health (NIH), National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT04188678
Brief Title
Resiliency in Older Adults Undergoing Bone Marrow Transplant
Acronym
REBOUND
Official Title
REBOUND: REsiliency in Older Adults UNDergoing BOne Marrow Transplant - A Pilot Study of Resiliency Measures in Older Patients Undergoing Allogeneic Blood and Marrow Transplant
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 28, 2018 (Actual)
Primary Completion Date
January 11, 2024 (Anticipated)
Study Completion Date
February 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Collaborators
National Institutes of Health (NIH), National Institute on Aging (NIA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The objective of this research is to measure certain indicators of resiliency to better understand which participants who are over 60 years old will respond more positively to bone marrow transplant. This research is being done to determine if there are traits that make recipients more likely to bounce back following allogeneic bone marrow transplant (BMT).
Detailed Description
Allogeneic blood and marrow transplantation (alloBMT) is the only potentially curative therapy for many forms of leukemia, lymphoma, and other hematologic malignancies. As with many forms of cancer, many of the most common indications for alloBMT disproportionally affect older people. Although treatments have improved for older adults undergoing therapies for these diseases, the outcomes are variable and there is little biological knowledge to help identify specific factors that would predict why some people do well with treatment and others develop functional and cognitive decline and other adverse health outcomes. Data specific to patients older than 60 who have undergone alloBMT are sparse even though the 1 year non-relapse mortality rate in patients older than age 50 at Johns Hopkins is 12%. In none of these studies have geriatric assessment measures in domains such as cognition and function been evaluated. Given the low incidence of non-relapse mortality in the investigators' older patients, the investigators have a unique opportunity to study the factors that influence not only mortality but function after hematopoietic stem cell transplantation. The investigators aim to be able to counsel patients more specifically about likely outcomes after transplant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leukemia, Lymphoma, Blood Cancer, Myelodysplastic Syndrome, Acute Myelogenous Leukemia, Non-Hodgkins Lymphoma
Keywords
Allogeneic blood and marrow transplantation (alloBMT), Resiliency, REBOUND, over age 60

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Age ≥60 years who are undergoing allogeneic bone marrow transplant at Johns Hopkins Hospital to treat a hematologic malignancy
Masking
None (Open Label)
Allocation
N/A
Enrollment
130 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Interventional Arm- Bone Marrow Transplant
Arm Type
Other
Arm Description
Study visits will include the performance of assessments prior to the start of conditioning chemotherapy and at 1 month and 6 months post-BMT. Assessments include: Physical function assessments questionnaires about general health and current health compared to health one year ago assessments that measure cognition, attention and memory assessments regarding personality and psychological and social stressors Physiological measures including blood tests- 160 mL of blood during evaluations, and 90mL of blood at the day 180 visit. bone marrow aspirate collected during standard of care bone marrow biopsies pre-transplant and at day 180 Saliva collections pre-transplant ACTH Stimulation Test Oral Glucose Tolerance Test Holter Monitor- to record hear rate variability MRI pre-transplant and at Day 180 in a subset of 10 subjects
Intervention Type
Other
Intervention Name(s)
Bone Marrow Transplant (BMT)
Intervention Description
Bone marrow transplantation will be conducted according to the investigators' institution's standard of care, or else according to research protocol (if applicable).Study visits that include the performance of assessments will occur prior to the start of conditioning chemotherapy and at 1 month and 6 months post-BMT. All dates are +/- 7 days. The initial study visit will take place during standard of care pre-transplant evaluations, which typically span 3-4 days. The post-BMT visits will take place before or after regularly-scheduled BMT follow up.
Primary Outcome Measure Information:
Title
Change in Physical Performance as assessed by Short Physical Performance Battery (SPPB)
Description
5 measured criteria: unintentional weight loss, exhaustion, low energy expenditure, low grip strength, and slowed waking speed. Scores of 3, 4 and 5 are consistent with frailty, scores of 1 and 2 are consistent with pre-frailty status, and a score of 0 is consistent with a robust or resilient status.
Time Frame
Pre-BMT, Day 30 and Day 180 post transplant
Title
Change in ability to perform activities of daily living as assessed by Instrumental Activities of Daily Living questionnaire
Description
questions about ability to perform activities of daily living (IADL). Scored low functioning (0) to high functioning (8).
Time Frame
Pre-BMT, Day 30 and Day 180 post transplant
Title
Change in upper extremity function as assessed by accelerometry
Description
device worn on wrist for a 24hr period that measures physical activity and sedentary activity. Higher scores= more active.
Time Frame
7 consecutive days pre-BMT, at Day 30 and at Day 180
Title
Change in catecholamines levels as assessed in overnight urine collection samples
Description
Changes in catecholamines level will be assessed in overnight urine collection samples. Levels fluctuate. Analysis will use the Johns Hopkins University (JHU) normal reference range for an adult is Metanephrine (normotensive):45-290 μg/24 hours. Metanephrine (hypertensive): 35-460 μg/24 hours .
Time Frame
Pre-BMT, Day 30 and Day 180 post transplant
Title
Change in Frailty as assessed by the Frailty Phenotype instrument
Description
Frailty Phenotype instrument is used to measure participants' walking speed and grip strength, includes questions about exhaustion, physical activity, weight loss. Higher scores indicate better functional state.
Time Frame
Pre-BMT, Day 30 and Day 180 post transplant
Title
Change in Pittsburgh Fatigability Scale for Older Adults score
Description
self-report tool that normalizes activities in terms of intensity and duration (PFS) this has a range of 0-50 with higher scores indicating greater physical fatigability.
Time Frame
Pre-BMT, Day 30 and Day 180 post transplant
Title
Change in Borg Rating of Perceived Exertion Scale score
Description
scale will be used immediately after a slow-paced 5-minute treadmill walk to assess fatigability (RPE). Higher score indicates higher perceived exertion.
Time Frame
Pre-BMT, Day 30 and Day 180 post transplant
Title
Change in medical history and diseases/conditions self reporting
Description
Questionnaire of past medical history as reported by a subject. This questionnaire does not have a score.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in health behaviors as assessed by a questionnaire
Description
This assessment is of self determined overall health as reported by a participant, it has no score.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in reporting of patients traumas as assessed by the Hospitalizations, Surgeries, and Falls Questionnaire
Description
Questionnaire includes items on hospitalizations, surgeries, and falls. it has no score.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in pain reporting as assessed by the Pain Assessment Questionnaire
Description
questions on overall bodily pain intensity/frequency and pain-related function/interference. Higher scores equal more pain.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in anxiety reporting as assessed by the anxiety questionnaire
Description
Questions to assess the presence and severity of anxiety; higher scores = more anxiety.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in trauma reporting as assessed by the trauma questionnaire
Description
Questions to assess a participants reporting of any past experiences of several kinds of trauma. It has no score.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in cognitive function as assessed by Modified Mini-Mental State Examination
Description
measure of global cognitive function (range 0-100). A score of 100 represents total cognitive function according to 3MS.
Time Frame
Pre-BMT, Day 30, Day 56 and Day 180 post transplant
Title
Change in cognitive ability as assessed by the Montreal Cognitive Assessment
Description
measures global cognitive function (MoCA). Scores range between 0 and 30. A score of 26 or over is considered to be normal.
Time Frame
Pre-BMT, Day 30, Day 56 and Day 180 post transplant
Title
Change in cognitive function as assessed by the Digit Symbol Substitution Test (DSST)
Description
participant fill in a series of symbols correctly coded within 90 seconds. The higher the score, the better the participant's performance.
Time Frame
Pre-BMT, Day 30, Day 56 and Day 180 post transplant
Title
Change in ability to cope with life challenges as assessed by the Coping Self-Efficacy Scale
Description
11-point Likert scale measures perceived ability to cope effectively with life. Scale is 0-10 with 10 = best ability to cope and 0 = no ability to cope.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in sense of well-being as assessed by the Subscale of Ryff Psychological Well-being Scale
Description
7-item Likert type scale (from strongly disagree to strongly agree) measures sense of direction and perception of purpose. Scale is 0-7 with 7 = best sense of well-being and 0 = no sense of well-being.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in perception and satisfaction with life as assessed by the Meaning in Life Questionnaire and Scale
Description
Likert-type scale measuring perception of meaning and satisfaction with life (MLQ) Scale is 0-7 with 7 = best sense that life has meaning and 0 = no sense that life has meaning.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in personality as measured by the Ten Item Personality Inventory (TIPI) Scale
Description
7 point Likert-type scale of disagree to agree with various aspects of personality measuring: extraversion, agreeableness, neuroticism, openness, conscientiousness. TIPI scale scoring. Extraversion: 1, 6R; Agreeableness: 2R, 7; Conscientiousness; 3, 8R; Emotional Stability: 4R, 9; Openness to Experiences: 5, 10R. ("R" denotes reverse-scored items)
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in optimism as assessed by the Life Orientation Scale-Revised
Description
5 point Likert scale, assessing optimism. 0= strongly disagree; 4 = strongly agree. The total score is from 0 to 24; higher scores indicate more optimism.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in perceived loneliness as assessed by the Loneliness Scale
Description
Revised University of California, Los Angeles (UCLA) Loneliness Scale. Each question is rated on a 4-point scale: 1 = never; 2 = Rarely; 3 = Sometimes 4 = Always. All items are summed to give a total score. Higher scores indicate more loneliness
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in perceived socio-economic status as assessed by the US socioeconomic questionnaire
Description
10-rung ladder to assess a participant's perception of participant's status in society. To score this measure, researchers simply note the number of the rung (1-10) on which the respondent placed their "X".
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in perceived financial strain as assessed by Financial Strain questionnaire
Description
2 item measure evaluating difficulty and anxiety about money. Higher scores equal higher financial strain.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in feeling of community inclusion as assessed by the Social Cohesion Questionnaire
Description
Participants rate their community by rate of agreement. Response is Agree a lot, a little, do not agree with 3 statements about their community.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in feeling of isolation as assessed by the Social Isolation/Engagement Questionnaire
Description
7-item measure evaluating social isolation, participation and engagement with others. Higher scores= greater sense of isolation.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in perceived confidence in spirituality as assessed by the Religion/Spirituality Questionnaire
Description
5-Item measure for use in epidemiological studies regarding spirituality. Score range from 5-27, with higher scores = more sense of spirituality
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in feelings of depression as assessed by the Patient Health Questionnaire
Description
Measures depressive symptoms in the last 2 weeks (PHQ-8)
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in perceived childhood trauma as assessed by the Adverse Childhood Events (ACE) Scale
Description
10-item measure to assess childhood abuse and household dysfunction. Response is yes/no. The ACE Scale is scored by summing the number of items for which respondents answered "yes."
Time Frame
Pre-BMT and Day 180 post transplant
Title
Changes in perceived stress as assessed by the Perceived Stress Scale
Description
5-point Likert scale measures the cognitive appraisal and perceptions of stress in life. Higher score= high level of perceived stress.
Time Frame
Pre-BMT and Day 180 post transplant
Title
Change in bone marrow cell ratios as assessed by Bone Marrow Aspirate
Description
aspirate will be collected during standard of care bone marrow biopsies and analyzed using JHU normal reference ranges.
Time Frame
pre-transplant and at Day 180 post-transplant
Title
Change in hemoglobin tests.
Description
160 mL of blood during evaluations, and 90mL of blood at the day 180 visit. Assessment will be documents using Hopkins normal reference ranges
Time Frame
pre-transplant and then at Day 30, Day 56 and Day 180 post-transplant
Title
changes in salivary plasma free cortisol collection
Description
Saliva collected at home by participants at 4 time points during a single 24 hour period. The mean salivary cortisol concentration is 15.5 +/- 0.8 nmol/L (range, 10.2-27.3) at 0800 h and 3.9 +/- 0.2 nmol/L (range, 2.2-4.1) at 2000 h.
Time Frame
single 24 hour period before BMT and at Day 180 post-transplant
Title
Change in cortisol level
Description
This is part of the ACTH Stimulation test to assess the reactivity of hypothalamic-pituitary-adrenal (HPA) axis. Test After the baseline blood draw is taken, 1mcg (low dose) Cosyntropin (synthetic ACTH) will be given intravenously by a research nursing staff followed by serial blood sampling to test for cortisol levels (mcg/dL).
Time Frame
pre-transplant and at Day 180 post-transplant
Title
Changes in interleukin (IL)-6 level
Description
This is part of the ACTH Stimulation test to assess the reactivity of HPA axis. After the baseline blood draw is taken, 1mcg (low dose) Cosyntropin (synthetic ACTH) will be given intravenously by a research nursing staff followed by serial blood sampling to test for IL-6 levels (pg/ml).
Time Frame
pre-transplant and at Day 180 post-transplant
Title
Change in dehydroepiandrosterone (DHEA) level
Description
This is part of the ACTH Stimulation test to assess the reactivity of HPA axis. After the baseline blood draw is taken, 1mcg (low dose) Cosyntropin (synthetic ACTH) will be given intravenously by a research nursing staff followed by serial blood sampling to test for DHEA levels (µg/dL).
Time Frame
pre-transplant and at Day 180 post-transplant
Title
Change in glucose tolerance as assessed by the Oral Glucose Tolerance Test (OGTT)
Description
Participants will fast overnight and then be given the 75 gram glucose oral load followed by blood draws at 0, 30. 60 and 120 minutes. At 120min, below 140mg/dL= normal blood sugar. 200mg/dL or higher= diabetes
Time Frame
pre-transplant and at Day 180 post-transplant
Title
Change in heart rate variability as assessed by the "myPatch" Holter monitor
Description
lightweight digital device that records and stores electrocardiogram (ECG) data on a continuous basis during study visits. A normal resting heart rate for adults ranges from 60 to 100 beats per minute. Generally, a lower heart rate at rest implies more efficient heart function.
Time Frame
During clinic visits at pre-transplant, Day 30, Day 56 and Day 180
Title
Change in attention as assessed by the Flanker Inhibitory Control and Attention Test score
Description
Measures attention and inhibitory control. Scoring is 0-10. Details and interpretations are available in the NIH toolbox scoring and interpretation guide.
Time Frame
pre-transplant, once a week from Day of transplant to Day 60 and at Day 180 post-transplant

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Undergoing allogeneic bone marrow transplant at Johns Hopkins Hospital, the indication for which is a hematologic malignancy Age ≥60 years Ability to walk without human assistance Enrollment in concomitant clinical research is permitted but not required English-speaking Ability to understand and the willingness to sign a written informed consent document. Exclusion Criteria: Unwillingness or inability to return at 6 months after transplantation for repeated evaluation Non-English-speaking
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philip Imus, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Resiliency in Older Adults Undergoing Bone Marrow Transplant

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