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Fitness Trial in Adults With Sickle Cell Disease (SCD Fit): A Feasibility Study

Primary Purpose

Cardiovascular Diseases, Sickle Cell Disease, Exercise

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise Sessions
Sponsored by
Memorial Healthcare System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Cardiovascular Diseases

Eligibility Criteria

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

Inclusion Criteria:

  • Participant must have sickle cell disease of any genotype
  • Participant must be 18 years of age
  • Participant must be seen and followed by the UAB sickle cell center
  • Participant must have reliable transportation to the UAB center of Exercise Medicine
  • Participant must be in steady-state disease (No vaso-occlusive crisis or SCD-related hospitalization with 4 weeks of enrollment)

Exclusion Criteria:

  • Participant has avascular necrosis
  • Participant is pregnant
  • Participant has absolute contraindications to exercise according to the American Heart Association and American College of Sports Medicine guidelines (42)

Sites / Locations

  • Memorial Healthcare System

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Exercise Treatment Group

Arm Description

Exercise Sessions

Outcomes

Primary Outcome Measures

Feasibility will be measured
Outcome will be to collect preliminary data on feasibility of the exercise intervention using rates of recruitment and retention
Acceptability will be measured
Outcome will be to collect preliminary data on acceptability of the exercise intervention using attendance, engagement, and qualitative feedback.
Tolerability will be measured
Outcome will be to collect preliminary data on tolerability of the exercise intervention using the ability for participants to complete the exercise program without adverse events.

Secondary Outcome Measures

Full Information

First Posted
February 23, 2021
Last Updated
December 6, 2022
Sponsor
Memorial Healthcare System
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1. Study Identification

Unique Protocol Identification Number
NCT04772391
Brief Title
Fitness Trial in Adults With Sickle Cell Disease (SCD Fit): A Feasibility Study
Official Title
Fitness Intervention Trial in Adults With Sickle Cell Disease (SCD Fit): A Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
September 1, 2022 (Actual)
Study Completion Date
October 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Memorial Healthcare System

4. Oversight

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

5. Study Description

Brief Summary
The purpose of this project is to develop novel approaches to promote health and longevity while enhancing quality of life among persons with Sickle cell disease (SCD). Therefore, investigators are aiming to adapt an evidence-based exercise intervention for adults with SCD informed by culturally- relevant and biologic factors and pre-test the adapted exercise program in a small sample of adults with SCD.
Detailed Description
Sickle cell disease (SCD) is a major public health concern as it is the most common inherited blood disorder in the US, affecting over 100,000 persons.(1) This disease predominantly affects African Americans, occurring in 1 out 365 African American births. Sickle cell disease causes intermittent extremely painful vaso-occlusion events, which lead to multi-organ damage, significant morbidity and early mortality - and resulting in increased healthcare utilization with estimated annual United States healthcare costs of 786 million.(2,3) To date, there are very few strategies for reducing pain, preventing organ dysfunction, and improving quality of life for persons with SCD leading to a disproportionate disparity in care. For this reason, there is a critical need to develop novel approaches to promote health and longevity while enhancing quality of life among persons with SCD. Exercise capacity and cardiorespiratory fitness are important predictors of cardiovascular outcomes and overall survival; however, adults with SCD have severely reduced levels of fitness, with less than 50% of expected compared to the general population. (4) Since cardiopulmonary disease accounts for 40% of the mortality in adults with SCD, enhancing physical activity with regular exercise is one potential method for improving survival, reducing poor Cardiovascular disease (CVD) outcomes, and improving quality of life for adults with SCD.(5,6) Evidence-based exercise interventions in rheumatoid arthritis, an inflammatory, chronic disease with similar sequelae to SCD, have shown that exercise interventions can increase quality of life, reduce pain, and improve CVD outcomes.(7-9) Currently, a paucity of research on the benefits of exercise for SCD exists and this is a critical barrier to overcome to both understand the role of physical fitness SCD and to develop evidence-based recommendations to guide exercise in SCD. Only one small study of an exercise intervention program in France has reported exercise to be safe, effective, and reverse SCD-related muscle vasculature damage but long term data in larger populations are needed.(10) Therefore, there is a need to conduct more studies in the United States and to develop an evidence-based exercise program for adults with SCD that integrates patient perspectives, can be broadly implemented among different settings, and is physically safe. To address this unmet need, the central hypothesis of this proposal is that an evidence-based exercise intervention informed by the needs and preferences of adults with SCD will be feasible, acceptable, and tolerable in a cohort of adults with SCD. Our long-term goal is to develop a safe and effective exercise intervention to promote sustainable physical activity in SCD and to guide exercise recommendations for SCD which currently do not exist. Therefore, investigators propose to adapt an evidence-based exercise intervention for adults with SCD informed by culturally- relevant and biologic factors and pre-test the adapted exercise program in a small sample of adults with SCD. Outcomes: The primary outcome will be to collect preliminary data on feasibility, acceptability, and tolerability of the exercise intervention. Rates of recruitment and retention will be measured to assess feasibility. Acceptability will be measured through attendance, engagement, and qualitative feedback. Tolerability will be measured by the ability for participants to complete the exercise program without adverse events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Sickle Cell Disease, Exercise

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise Treatment Group
Arm Type
Other
Arm Description
Exercise Sessions
Intervention Type
Other
Intervention Name(s)
Exercise Sessions
Intervention Description
Participant will complete up to 8 exercise sessions
Primary Outcome Measure Information:
Title
Feasibility will be measured
Description
Outcome will be to collect preliminary data on feasibility of the exercise intervention using rates of recruitment and retention
Time Frame
One year
Title
Acceptability will be measured
Description
Outcome will be to collect preliminary data on acceptability of the exercise intervention using attendance, engagement, and qualitative feedback.
Time Frame
One year
Title
Tolerability will be measured
Description
Outcome will be to collect preliminary data on tolerability of the exercise intervention using the ability for participants to complete the exercise program without adverse events.
Time Frame
One year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participant must have sickle cell disease of any genotype Participant must be 18 years of age Participant must be seen and followed by the UAB sickle cell center Participant must have reliable transportation to the UAB center of Exercise Medicine Participant must be in steady-state disease (No vaso-occlusive crisis or SCD-related hospitalization with 4 weeks of enrollment) Exclusion Criteria: Participant has avascular necrosis Participant is pregnant Participant has absolute contraindications to exercise according to the American Heart Association and American College of Sports Medicine guidelines (42)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Foluso Ogunsile, MD
Organizational Affiliation
Memorial Healthcare System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Memorial Healthcare System
City
Hollywood
State/Province
Florida
ZIP/Postal Code
33021
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
To be determined

Learn more about this trial

Fitness Trial in Adults With Sickle Cell Disease (SCD Fit): A Feasibility Study

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