Impact of Prehabilitation in Oncology Via Exercise- Bone Marrow Transplant

Physical Activity Clinical Trial

— IMPROVE-BMT  

Official title:

The Effects of a Prehabilitation Exercise Program in Adults Receiving a Hematopoietic Stem Cell Transplant

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03886909
• Other study ID #: STUDY00010914
• Status: Completed
• Phase: N/A
• Start date: June 28, 2019
• Est. completion date: April 13, 2023

Study information

• Verified date: July 2023
• Source: Milton S. Hershey Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether patients are able to participate in a prehabilitation program (prior to the beginning of treatment) which includes: (1) a home-based exercise program or (2) just a prehabilitation education session.

Description:

Hematopoietic stem cell transplant may have the potential for severe side effects, including functional (reduced aerobic capacity, reduced muscle strength) and psychosocial (e.g. reduced quality of life, increased fatigue) detriments.

Evidence shows that exercise is considered to be an effective treatment approach in hematopoietic stem cell transplant patients during and after treatment with regard to the above mentioned side-effects. Also, prehabilitative exercise in colon and lung cancer patients was shown as feasible and effective. However, no experience exists with regard to prehabilitation exercise in hematopoietic stem cell transplant patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 84
• Est. completion date: April 13, 2023
• Est. primary completion date: April 13, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Hematological cancer (e.g. Acute Myeloid Leukemia, Chronic Lymphocytic Leukemia, Multiple Myeloma, Non-Hodgkin Lymphoma, etc.)

• Hematological cancer in remission

• Females and males =18 years of age

• Fluent in written and spoken English

• Must be able to provide and understand informed consent

• Must have an ECOG score of = 2

• Scheduled for an inpatient autologous or allogeneic stem cell transplant at Penn State Cancer Institute

• = 2 weeks until scheduled transplant

• Primary attending physician approval

Exclusion Criteria:

• Hematological cancer not in remission

• Evidence in the medical record of an absolute contraindication (e.g. Heart insufficiency > NYHA III or uncertain arrhythmia; uncontrolled hypertension; reduced standing or walking ability) for exercise

• Any other comorbidities or musculoskeletal complications that preclude participation in the exercise programs as deemed by the exercise interventionist

• Uncontrolled hypertension

• Receiving non-transplant related chemotherapy and/or radiotherapy

• Not fluent in written and spoken English

• Active infections, hemorrhages, and cytopenias that could place transplant patients at risk for further adverse events, deemed by the exercise interventionist, physician and/or nurse

Related Conditions & MeSH terms

• Hematologic Diseases
• Hematopoietic Stem Cell Transplant
• Physical Activity
• Prehabilitation

Intervention

Behavioral:
• Exercise
The exercise intervention is at least 2 weeks lasting (till the day transplant is taking place) 5-times weekly resistance training intervention combined with aerobic exercise (mostly walking).
• Prehabilitation Education
Participant will receive a prehabilitation and stem cell education class which will be held at the Penn State Cancer Institute.

Locations

Country	Name	City	State
United States	Penn State Cancer Institute	Hershey	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Milton S. Hershey Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of the exercise intervention: 50% of included patients actually complete at least one third of the exercise sessions	The exercise intervention will be considered feasible if 50% of included patients actually complete at least one third of the exercise sessions prescribed for 2 weeks or more.	Through study completion, an average of 18 months
Primary	Acceptability of the exercise intervention: more than 50% of the patients approached	The exercise intervention will be considered acceptable if more than 50% of the patients approached agree to receive at least the first exercise session.	During recruitment
Primary	Safety of the exercise intervention: questionnaire	Within the questionnaire we will assess whether musculoskeletal occur (yes/no; ongoing; location; severity (mild-life threatening); daily activities affected). The intervention will be considered as safe if less than 25% of included patients report mild musculoskeletal impairments and less than 5% experienced musculoskeletal injuries (defined as symptoms lasting a week or longer and or requiring the attention of a medical professional).	Through the study completion, an average of 18 months
Secondary	Health-related Quality of Life: European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30, version 3.0)	QoL will be assessed with the validated 30-item self-assessment questionnaire of the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30, version 3.0).; The QLQ-C30 is composed of both multi-item scales and single-item measures. These include five functional scales, three symptom scales, a global health status / QoL scale, and six single items. Each of the multi-item scales includes a different set of items - no item occurs in more than one scale. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. Thus a high score for a functional scale represents a high / healthy level of functioning, a high score for the global health status / QoL represents a high QoL, but a high score for a symptom scale / item represents a high level of symptomatology / problems.	Through study completion, an average of 18 months
Secondary	Bone Marrow Transplant-related Quality of Life: EORTC QLQ-HDC29	Quality of Life will be assessed with the validated 29-item self-assessment questionnaire of the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire- High Dose Chemotherapy- 29 Items (EORTC QLQ-HDC29).; The QLQ HDC29 module includes 29 items, consisting of six multi-item scales and eight single-items. For the multi-item scales and single-item scales a high score is equivalent to worse or more symptoms/problems.	Through study completion, an average of 18 months
Secondary	Fatigue	Fatigue will be assessed with the Multidimensional Fatigue Inventory (MFI) which is a 20-item, multidimensional self-assessment questionnaire.; Respondents use a scale ranging from 1 to 7 to indicate how aptly certain statements regarding fatigue represent their experiences. Higher total scores correspond with more acute levels of fatigue.	Through study completion, an average of 18 months
Secondary	Sleep	Sleep quality and sleep problems will be assessed with the validated and frequently used Pittsburgh Sleep Quality Index (PSQI).; In scoring the PSQI, seven component scores are derived, each scored 0 (no difficulty) to 3 (severe difficulty). The component scores are summed to produce a global score (range 0 to 21). Higher scores indicate worse sleep quality.	Through study completion, an average of 18 months
Secondary	Depression	Depressive symptoms will be assessed with the 20-item Center for Epidemiological Studies Depression Scale (CES-D).; Zero for 'Rarely', 1 for 'Some or a little of the time', 2 for 'Occasionally or a moderate amount of time', 3 for 'Most or all of the time'. Possible range of scores is zero to 60, with the higher scores indicating the presence of more symptomatology.	Through study completion, an average of 18 months
Secondary	Short Questionnaire to Assess Health-Enhancing Physical Activity	Physical activity behavior in the domains of commuting activity, leisure time activities such as cycling, walking, and sports, household and occupational activity will be assessed via a standardized and validated questionnaire, the Short QUestionnaire to ASsess Health-enhancing Physical Activity (SQUASH).; Household work and activities at work or school were prestructured for intensity. A basic intensity score of 2 and 5 for light and intense activities, respectively. Total minutes of activity are calculated for each question by multiplying frequency (days/week) by duration (min/day). Activity scores for separate questions are calculated by multiplying total minutes of activity by the intensity score. The total activity score is calculated by taking the sum of the activity scores for separate questions. Higher values equals more time spent completing the activity.	Through study completion, an average of 18 months
Secondary	Godin Physical Activity Questionnaire	Physical activity behavior in the domains of commuting activity, leisure time activities such as cycling, walking, and sports, household and occupational activity will be assessed via a standardized and validated questionnaire, the Godin Physical Activity Questionnaire.; Total weekly leisure activity is calculated in arbitrary units by summing the products of the separate components, as shown in the following formula: Weekly leisure activity score = (9 × Strenuous) + (5 × Moderate) + (3 × Light) Higher activity score = more active	Through study completion, an average of 18 months
Secondary	Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events	Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) will be used to collect information on severity and interference of symptoms and adverse events.	Through study completion, an average of 18 months
Secondary	Body Pain: Brief Pain Inventory- Short form	Bodily pain will be assessed using the Brief Pain Inventory- Short form (BPI-SF).; The BPI gives two main scores: a pain severity score and a pain interference score. The pain severity score is calculated from the four items about pain intensity. Each item is rated from 0, no pain, to 10, pain as bad as you can imagine, and contributes with the same weight to the final score, ranging from 0 to 40. The pain interference score corresponds to the item on pain interference. The seven sub-items are rated from 0, does not interfere, to 10, completely interferes, and contributes with the same weight to the final score, ranging from 0 to 70.	Through study completion, an average of 18 months
Secondary	Physical Function: Short Physical Performance Battery	Objectively-measured physical function will be assessed using the Short Physical Performance Battery (SPPB).; The SPPB is an accumulation of balance tests, 4-meter gait speed, and 5-chair stands. Based on the time needed to complete the chair stands, a score is given. A summation of scores from all tests is taken, ranging from 0 -12. A higher score = Higher physical function.	Through study completion, an average of 18 months
Secondary	Aerobic Capacity: Six Minute Walk Test	Objectively-measured physical function will be assessed using the Six Minute Walk Test (6MWT).; Distance walked during 6 minutes (measured in meters) is measured. Longer distance = higher aerobic capacity.	Through study completion, an average of 18 months
Secondary	Physical Function: Timed-Up-and-Go Test	Objectively-measured physical function will be assessed using the Timed-Up-and-Go test (TUG).; Time taken to stand up from a chair, walk 10 meters around an obstacle, and return to seated position is measured in seconds. Lower time = better physical function.	Through study completion, an average of 18 months
Secondary	Fall Risk	Functional balance will be assessed using the Berg Balance Scale.; Scoring: A five-point ordinal scale, ranging from 0-4. "0" indicates the lowest level of function and "4" the highest level of function. Score is summation of all items. Highest Total Score = 56 Interpretation: 0-20: Wheelchair bound; 21-40: Walking with assistance; 41-56: Independent	Through study completion, an average of 18 months