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Trial record 9 of 25 for:    spinal cord injury AND NICHD

Feasibility of Exercise and Spinal Cord Injury

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ClinicalTrials.gov Identifier: NCT03941600
Recruitment Status : Recruiting
First Posted : May 8, 2019
Last Update Posted : May 8, 2019
Sponsor:
Collaborator:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Information provided by (Responsible Party):
Kerri Morgan, Washington University School of Medicine

Brief Summary:
The purpose of the study is to examine the impact of a community-based exercise intervention (CBEI) for persons with spinal cord injury (PwSCI) on physiological and psychological well-being and identify barriers and facilitators to implementation.

Condition or disease Intervention/treatment Phase
Spinal Cord Injuries Behavioral: Community-based Exercise Intervention group (CBE) Behavioral: Exercise Education Control group (EEG) Not Applicable

Detailed Description:

People with spinal cord injury (PwSCI) are at a greater risk for major health conditions and poorer health outcomes than the population without spinal cord injury. For PwSCI, habitual exercise is critical for both physiological and psychological well-being. Prior research indicates that exercise programs conducted in a controlled setting have positive effects on the physical and psychosocial fitness of PwSCI, but the efficacy and feasibility of these programs are not well understood in community-based settings. The proposed project aims to examine potential health benefits in response to the intervention and identify the barriers and facilitators to successful implementation of a CBEI in PwSCI. The long-term goal of this research is to improve health outcomes of PwSCI by identifying strategies to promote health and support exercise in the community.

The project research aims are to:

  1. Estimate improvements in physical function, cardio-metabolic health, and psychological well-being of participants enrolled in a CBEI compared to an education-only group.
  2. Identify barriers, facilitators, and reasons for positive determinants for PwSCI to exercise in a community-based setting.

A single-blind pilot RCT will be conducted. Forty individuals with SCI will be recruited. Each participant will be randomized into either a 12-week CBEI (n=20) or an education control group (n=20). Participants' cardiorespiratory fitness, body composition, metabolic blood chemistries and strength will be assessed pre- (T1) and post- (T2) intervention.


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Feasibility of a Community-based Exercise Intervention for Persons With Spinal Cord Injury
Actual Study Start Date : April 10, 2019
Estimated Primary Completion Date : August 30, 2020
Estimated Study Completion Date : August 30, 2020

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Active Comparator: Community-based Exercise Intervention group (CBEI)
A group performing a 12-week guided exercise program at an accessible community health and wellness center
Behavioral: Community-based Exercise Intervention group (CBE)
The CBEI group will receive 36 (60-90 minute) one-on-one, formally directed exercise sessions by trained staff over 12 weeks. By the end the goal is to have the participants guiding their own regimens. Personalized sessions will be created for each participant based on their fitness goal(s) and preferences. Each session will include vitals, pain assessment, warm-up, stretching, cardiovascular, and strength exercises and cool-down. The participants will be monitored to ensure they are achieving at least 30 minutes of moderate-to-vigorous exercise 3 times a week. Activity monitors will also be worn to capture intensity data. At the end of each session, participants will describe their likes and dislike as well as what they gained and what they suggest for improvement. At the end of each session, the trainer will rate the participant's perceived participation during the session (1-6) using the Pittsburgh Rehabilitation Participation Scale.

Placebo Comparator: Exercise Education Control group (EEG)
A group receiving educational information about physical activity and exercise at home and then self-direction a 12-week exercise program on their own.
Behavioral: Exercise Education Control group (EEG)
The EEG group will complete an intervention that consists of a one-on-one, hour-long educational session orienting participants to an online resource center, the National Center on Health, Physical Activity, and Disability (NCHPAD). NCHPAD promotes health and well-being for PwD through resources such as adapted exercise videos, information on accessible fitness equipment, personalized exercise videos tailored to PwD, and an individualized 14-week exercise program. Participants will be given an overview of NCHPAD and asked to identify resources of interest on the website. Each participant will be asked to use resources on NCHPAD to engage in physical activity for 12 weeks. Each participant will receive a weekly phone call to inquire about their physical activity, exercises engaged in, RPE during exercise, and whether any resources were used.




Primary Outcome Measures :
  1. VO2 peak - Cardiorespiratory fitness change (peak oxygen consumption change) [ Time Frame: Baseline and Up to 4 weeks post intervention ]
    VO2 peak will be measured using a standard computer-integrated, open-circuit, breath-by-breath metabolic measurement system (TrueOne 2400, Parvo Medics, Sandy UT) while the participant performs a graded-exercise test on an arm crank ergometer (SCIFIT PRO2, Life Fitness, Tulsa, OK). The protocol involves a 3-minute warm-up followed by a standard ramp protocol which is typically completed in 8-12 minutes.

  2. DEXA - Body composition overall body fat % change [ Time Frame: Baseline and Up to 4 weeks post intervention ]
    Participants will then undergo body composition assessment via DEXA (General Electric Lunar iDXA), which is commonly used in research due to its precision and safety. Body fat % will be the unit of measure.

  3. Metabolic blood chemistries - HbA1c level change [ Time Frame: Baseline and Up to 4 weeks post intervention ]
    Blood draws will be completed to measure HbA1c levels in %. Participants will fast 8-10 hours prior to blood draw.

  4. Metabolic blood chemistries - Cholesterol change [ Time Frame: Baseline and Up to 4 weeks post interventions ]
    Blood draws will be completed to measure cholesterol levels. Unit of measure will be in mg/dL. Participants will fast 8-10 hours prior to blood draw.


Secondary Outcome Measures :
  1. Upper extremity strength - upper body strength change [ Time Frame: Baseline and Up to 4 weeks post intervention ]
    Strength will be measured via isotonic 1RM testing unilaterally on four upper-extremity exercises (chest press, back row, rickshaw, biceps flexion) using a BTE™ PrimusRS (BTE™, Hanover, MD).

  2. PROMIS - Fatigue Short Form 8a [ Time Frame: Baseline and Up to 4 weeks post intervention ]

    The Fatigue item banks assess a range of self-reported symptoms, from mild subjective feelings of tiredness to an overwhelming, debilitating, and sustained sense of exhaustion that likely decreases one's ability to execute daily activities and function normally in family or social roles. Fatigue is divided into the experience of fatigue and the impact of fatigue. The fatigue short forms are not disease specific and assess fatigue over the past seven days. PROMIS instruments are scored using item-level calibrations. Each question is answered using a 5-point Likert scale from "not at all (1)" to "very much (5)". Calculate a summed score and then use the applicable PROMIS score conversion table to translate the total raw score into a T-score.

    The seven domains are scored individually, and the single pain intensity item is reported as its raw score.


  3. PROMIS - Emotional Distress - Depression - Short Form 8a [ Time Frame: Baseline and Up to 4 weeks post intervention ]

    The Depression item banks assess self-reported negative mood (sadness, guilt), views of self(self-criticism, worthlessness), and social cognition (loneliness, interpersonal alienation), as well as decreased positive affect and engagement (loss of interest, meaning, and purpose). The depression short forms are not disease specific and assess depression over the past seven days. PROMIS instruments are scored using item-level calibrations. Each question is answered using a 5-point Likert scale from "never (1)" to "always (5)". Calculate a summed score and then use the applicable PROMIS score conversion table to translate the total raw score into a T-score.

    The seven domains are scored individually, and the single pain intensity item is reported as its raw score.


  4. PROMIS - Pain Intensity - Short Form 3a [ Time Frame: Baseline and Up to 4 weeks post intervention ]

    The Pain Intensity instruments assess how much a person hurts. The pain intensity short forms are not disease specific and assess pain intensity over the past seven days. PROMIS instruments are scored using item-level calibrations. Each question is answered using a 5-point Likert scale from "Had no pain (1)" to "very severe (5)". Calculate a summed score and then use the applicable PROMIS score conversion table to translate the total raw score into a T-score.

    The seven domains are scored individually, and the single pain intensity item is reported as its raw score.


  5. PROMIS - Pain Interference - Short Form 8a [ Time Frame: Baseline and Up to 4 weeks post intervention ]

    The Pain Interference item banks assess self-reported consequences of pain on relevant aspects of one's life. This includes the extent to which pain hinders engagement with social, cognitive, emotional, physical, and recreational activities. It also incorporates items probing sleep and enjoyment in life. The pain interference short forms are not disease specific and assess pain interference over the past seven days. PROMIS instruments are scored using item-level calibrations. Each question is answered using a 5-point Likert scale from "not at all (1)" to "very much (5)". Calculate a summed score and then use the applicable PROMIS score conversion table to translate the total raw score into a T-score.

    The seven domains are scored individually, and the single pain intensity item is reported as its raw score.


  6. PROMIS - Sleep Disturbance - Short Form 8a [ Time Frame: Baseline and Up to 4 weeks post intervention ]

    The Sleep disturbance instruments assess self-reported perceptions of sleep quality, sleep depth, and restoration associated with sleep. This includes perceived difficulties and concerns with getting to sleep or staying asleep, as well as perceptions of the adequacy of and satisfaction with sleep. The sleep disturbance short forms are not disease specific and assess sleep disturbances over the past seven days. PROMIS instruments are scored using item-level calibrations. Each question is answered using a 5-point Likert scale from "very poor (1)" to "very good (5)". Calculate a summed score and then use the applicable PROMIS score conversion table to translate the total raw score into a T-score.

    The seven domains are scored individually, and the single pain intensity item is reported as its raw score.


  7. PROMIS - Emotional Support [ Time Frame: Baseline and Up to 4 weeks post intervention ]

    The Emotional support item banks assess perceived feelings of being cared for and valued as a person; having confident relationships. PROMIS instruments are scored using item-level calibrations. Each question is answered using a 5-point Likert scale from "never (1)" to "always (5)". Calculate a summed score and then use the applicable PROMIS score conversion table to translate the total raw score into a T-score.

    The seven domains are scored individually, and the single pain intensity item is reported as its raw score.




Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosis of SCI
  • 18 years or older
  • Have written physician approval to participate in the study
  • Ability to use upper extremities to exercise
  • Participate in < 60 minutes of moderate-intensity exercise per week in the last month
  • Understand English at a sixth-grade level or higher
  • Be able to follow multi-step instructions
  • Independently provide informed consent
  • Willing to participate in three assessments and 36 intervention sessions

Exclusion Criteria:

  • Enrollment in a structured exercise program in the past six months.
  • Have had cardiovascular complications within the past year
  • Currently receive medical treatment for an acute upper extremity injury
  • Have a Stage IV pressure injury
  • Have a cognitive impairment that does not allow them to provide consent or follow multi-step directions.

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): NCT03941600


Contacts
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Contact: Kimberly A Walker, OTD 314-273-7010 walker.k@wustl.edu
Contact: Kerri A Morgan, PhD 314-286-1659 morgank@wustl.edu

Locations
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United States, Missouri
Washington University School of Medicine Recruiting
Saint Louis, Missouri, United States, 63108
Contact: Kimberly A Walker, OTD    314-273-7010    walker.k@wustl.edu   
Contact: Kerri A Morgan, PhD    314-286-1659    morgank@wustl.edu   
Sponsors and Collaborators
Washington University School of Medicine
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Investigators
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Principal Investigator: Kerri A Morgan, PhD Washington University School of Medicine

Publications:
National Spinal Cord Injury Statistical Center. (2016). 2016 Annual Statistical Report - Complete Public Version. Birmingham, AL: University of Alabama at Birmingham.
Kaye, H. S., Kang, T., & LaPlante, M. P. (2000). Mobility device use in the United States. (No. 14). Washington, DC: U.S. Department of Education, National Institute on Disability and Rehabilitation Research.
American College of Sports Medicine. (2014). ACSM's Guidelines for Exercise Testing and Prescription (9th ed.). Philadelphia: Lippincott Williams & Wilkins.
U.S. Department of Health and Human Services (2008). 2008 Physical Activity Guidelines for Americans. Washington, D. C.: U.S. Department of Health and Human Services.
Krueger, R. A. & Casey, M. A. (2009). Focus Groups: A Practical Guide for Applied Research (4th ed.). Thousand Oaks, CA: Sage.

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Responsible Party: Kerri Morgan, Assistant Professor of Occupational Therapy and Neurology, Washington University School of Medicine
ClinicalTrials.gov Identifier: NCT03941600     History of Changes
Other Study ID Numbers: 201809174
K12HD055931 ( U.S. NIH Grant/Contract )
First Posted: May 8, 2019    Key Record Dates
Last Update Posted: May 8, 2019
Last Verified: May 2019

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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 Kerri Morgan, Washington University School of Medicine:
occupational therapy
exercise
Additional relevant MeSH terms:
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Spinal Cord Injuries
Wounds and Injuries
Spinal Cord Diseases
Central Nervous System Diseases
Nervous System Diseases
Trauma, Nervous System