- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03411720
Whole Body Exercise in Spinal Cord Injury: Effects on Psychosocial Function
19. juni 2020 opdateret af: J. Andrew Taylor, Spaulding Rehabilitation Hospital
Persons with spinal cord injury (SCI) are confronted with a multitude of psychological and physiological changes post-injury leading to seemingly insurmountable barriers to participating in daily life.
After injury persons with SCI engage in fewer social interactions, spend more time sedentary, and are less likely to leave the home.
This leads to restricted social participation that, in turn, contributes to greater psychological problems and negatively impacts the lives of adults with SCI.
Intense, structured exercise has substantial potential benefits for improving psychosocial wellbeing among persons with SCI, but accessible exercise options are few and cannot achieve high intensities of whole-body exercise.
This work will use approaches to overcome the barriers to intense exercise.
The investigators will use hybrid functional electrical stimulation row training (FESRT) to allow for a more intense exercise stimulus, potentially having a greater impact on psychosocial wellbeing.
There is initial evidence that persons with mobility impairments who are highly physically active demonstrate better psychosocial wellbeing compared with those who have low levels of physical activity.
A limitation to understanding the influence of exercise on psychosocial wellbeing is the lack of robust and time-dependent measures.
The investigators will use a smartphone-based research application to measure psychosocial well-being, thus decreasing self-report bias and capturing in-the-moment behavioral and self-report data.
Studieoversigt
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
26
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Massachusetts
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Cambridge, Massachusetts, Forenede Stater, 02139
- Spaulding Rehabilitation Network
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
Adults (>18 years of age)
- Be in good health (asymptomatic for acute treatable illness) and medically cleared to exercise
- Own an iPhone or Android smartphone with the capacity to download and run the research platform (able to log into to the relevant app store, install the app on their own phone, and run the app).
- Be able to understand, communicate with and be understood by research personnel or Interpreters
- Be interested in participating and provide informed consent
- Have a SCI with motor or sensory deficits and use a wheelchair as primary means of mobility
- Have an injury level only as high as C4 to allow sufficient arm function for rowing
Exclusion Criteria:
- Participants will not have previously completed FESRT
- Acute illness
- Musculoskeletal injuries that have not healed completely
- Had heart surgery or are status post-myocardial infarction (MI) in the last 4 to 6 months, -Unstable angina
- Uncontrolled hypertension (systolic blood pressure ≥160 mm Hg and/or diastolic blood pressure ≥100 mm Hg)
- uncontrolled dysrhythmias
- Recent history of congestive heart failure that has not been evaluated and effectively treated
- Severe stenotic or regurgitant valvular disease
- Hypertrophic cardiomyopathy
- Unhealed pressure ulcer Stage 2 or higher at relevant contact sites during exercise.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: FES-row-training
Subjects will perform 4 months of FES-row-raining
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Hybrid FES Row Training using voluntary upper body and electrically-stimulated lower body
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Andet: Wait-list time control
Subjects will wait 4 months before performing being allowed to engage in 4 months of FES-row-training
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Hybrid FES Row Training using voluntary upper body and electrically-stimulated lower body
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Aktiv komparator: Arms-only-row-training
Subjects will perform 4 months of arms-only row training before being allowed to engage in 4 months of FES-row-training
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Hybrid FES Row Training using voluntary upper body and electrically-stimulated lower body
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Depression
Tidsramme: Each week during the 4 months
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Difference between groups in depression symptom severity (Patient Health Questionnaire-9); Within-individual Correlation of exercise intensity with depression
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Each week during the 4 months
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Pain Severity
Tidsramme: Each week during the 4 months
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Difference between groups in pain severity, rated on a 0-10 scale ("0 being no pain and 10 being pain so severe you couldn't stand it"); Within-individual Correlation of exercise intensity with pain.
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Each week during the 4 months
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Pain Interference
Tidsramme: Each week during the 4 months
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Difference between groups in pain interference in daily life activities ("0.
Not at all 1.
A little bit 2. Moderately 3. Quite a bit 4. Extremely"); Within-individual Correlation of exercise intensity with pain.
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Each week during the 4 months
|
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Anxiety
Tidsramme: Each week during the 4 months
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Difference between groups in anxiety (Spinal Cord Injury Quality of Life Anxiety Short Form); Within-individual Correlation of exercise intensity with anxiety.
Minimum score is 9, Maximum score is 45.
Higher scores indicate higher anxiety.
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Each week during the 4 months
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Satisfaction with Social Participation
Tidsramme: Each week during the 4 months
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Difference between groups in satisfaction with social roles and activities (Spinal Cord Injury Quality of Life Satisfaction with Social Roles and Activities Short Form); Within-individual Correlation of exercise intensity with satisfaction with social participation.
The Minimum score is 20 and the maximum score is 50.
Higher values indicate greater satisfaction with social participation.
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Each week during the 4 months
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Ability to participate in social roles
Tidsramme: Each week during the 4 months
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Difference between groups in ability to participate in social roles and activities.
Spinal Cord Injury Quality of Life Ability to Participate in Social Roles and Activities Short Form.
Within-individual Correlation of exercise intensity with ability to participate in social roles.
The Minimum score is 20 and the maximum score is 50.
Higher values indicate greater satisfaction with social participation.
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Each week during the 4 months
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Health Complications
Tidsramme: Each week during the 4 months
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Difference between groups in frequency of secondary health complications; Within-individual Correlation of exercise intensity with secondary health complications.
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Each week during the 4 months
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Community Mobility
Tidsramme: Each week during the 4 months
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Difference between groups in community mobility (Distance traveled each week); Within-individual Correlation of exercise intensity with community mobility.
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Each week during the 4 months
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Social Connectivity: Frequency
Tidsramme: Each week during the 4 months
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Difference between groups in social connectivity (Frequency of phone calls and text messages); Within-individual Correlation of exercise intensity with frequency of social connectivity.
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Each week during the 4 months
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Social Connectivity: Reciprocity
Tidsramme: Each week during the 4 months
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Difference between groups in social connectivity (Reciprocity of phone calls and text messages); Within-individual Correlation of exercise intensity with reciprocity of social connectivity.
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Each week during the 4 months
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: J. Andrew Taylor, Spaulding Rehabilitation Hospital/Harvard Medical School
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
28. februar 2018
Primær færdiggørelse (Faktiske)
31. maj 2020
Studieafslutning (Faktiske)
31. maj 2020
Datoer for studieregistrering
Først indsendt
5. januar 2018
Først indsendt, der opfyldte QC-kriterier
25. januar 2018
Først opslået (Faktiske)
26. januar 2018
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
22. juni 2020
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. juni 2020
Sidst verificeret
1. juni 2020
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2017D006049
Plan for individuelle deltagerdata (IPD)
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