Telerehabilitation and Lymphoma Patients
19. juli 2022 opdateret af: Ladislav Batalik, Brno University Hospital
Effect of the Physical Exercise Training Using Telerehabilitation Among Lymphoma Patients: A Pilot Study
This study aims to examine the feasibility and effect of a home-based short-term telerehabilitation exercise intervention using heart rate monitor and internet platform in patients with lymphoma.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Fifteen lymphoma cancer patients post-treatment (except adjuvant treatment) will be enrolled in the study.
Cardiorespiratory fitness (peak oxygen consumption), adverse events, body composition and adherence to exercise prescription will be evaluated at baseline, 12-week, and year after enrollment.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
15
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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Brno, Tjekkiet, 62500
- University Hospital Brno
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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:
- Lymphoma patients post-treatment (except ongoing adjuvant treatment)
- Post-treatment period not exceeding 3 months
- Internet connection at home
- Literacy with information and communication technology
- Patients who agreed with informed consent
Exclusion Criteria:
- Inability to perform a cardiopulmonary exercise test
- Psychological severe or cognitive disorders
- Contraindications for cardiopulmonary exercise testing
- Other exercise limitations (musculoskeletal disorders)
- Planned intervention or operation
- Participants who are enrolled in or participate in other rehabilitation program
- Participants who plan to be or are included in other studies
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: Home-based telerehabilitation exercise
Exercise training is conducted in the patient's home conditions using modern technology to transfer medical data remotely - the participants receive a heart rate monitor and sensor.
To know what to do and how to exercise, the first (1-2) exercise training sessions will be controlled by the physiotherapist in a rehabilitation clinic in the hospital, who creates individual exercise training for each patient.
The patient's training data will be downloaded and updated regularly via the internet platform and clinicians will evaluate these results and provide patients with telephone feedback.
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Eligible participants will undergo 12 weeks of physical exercise using a heart rate monitor and internet platform at home.
The participants will regularly (minimum once per week) upload the exercise data from the heart rate monitor into the internet platform.
An exercise telerehabilitation session consists of the warm-up phase, aerobic phase (30 - 50 minutes gradually increasing exercise duration; heart rate zone based on baseline cardiopulmonary exercise test) and cool-down phase.
The exercise training period is set to 3 times a week for 12 weeks.
Study participants will receive user guides developed by research team with detailed instructions regarding equipment set-up, training protocol, and contact information.
Also, participants will receive weekly phone calls from week 0 to week 12 to monitor adverse events, encourage compliance and adherence to the study protocol, address any subject questions or concerns, and collect information regarding participants' current symptomatology.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Cardiorespiratory fitness (CRF)
Tidsramme: Change from baseline to 12 weeks and 1-year
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Peak oxygen uptake (VO2peak) during the cardiopulmonary exercise test
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Change from baseline to 12 weeks and 1-year
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Body composition (Total muscle mass in kilograms)
Tidsramme: Change from baseline to 12 weeks and 1-year
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Total muscle mass is the amount of muscle in body, including skeletal muscles, smooth muscles, and cardiac muscles.
Total muscle mass will be measured by bioelectrical impedance analysis.
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Change from baseline to 12 weeks and 1-year
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Body composition (Body fat mass in kilograms)
Tidsramme: Change from baseline to 12 weeks and 1-year
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Body fat mass is the actual weight of fat in body.
Body fat mass will be measured by bioelectrical impedance analysis.
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Change from baseline to 12 weeks and 1-year
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Body composition (Body weight in kilograms)
Tidsramme: Change from baseline to 12 weeks and 1-year
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Body weight is the measurement of weight without items located on the person.
Body weight will be measured by bioelectrical impedance analysis.
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Change from baseline to 12 weeks and 1-year
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Incidence of treatment-emergent adverse events assessed by 5 grade scale
Tidsramme: Data will be recorded continuously from the baseline to 12 weeks
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Participants will be encouraged to use the contact details for reporting the incidence of treatment-emergent adverse events at any time throughout the study period.
The type, incidence, and severity of adverse events by scale (Grade 1: Mild, asymptomatic or mild symptoms; Grade 2: Moderate, minimal; Grade 3: Severe or medically significant; Grade 4: Life-threatening consequences; and Grade 5: Death) will be noted
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Data will be recorded continuously from the baseline to 12 weeks
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Exercise adherence
Tidsramme: 12 weeks
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Exercise adherence is defined as number of exercise sessions attended of a possible 36 offered by the exercise intervention program.
Exercise adherence will be determined by participant exercise web datasheet review at 12 weeks.
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12 weeks
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Exercise compliance
Tidsramme: 12 weeks
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Number of participants who attend atleast 70% of prescribed exercise sessions measured by exercise datasheet at 12 weeks.
(70% of prescribed exercise sessions = 25 exercise sessions in 12 weeks)
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12 weeks
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
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)
1. april 2021
Primær færdiggørelse (Faktiske)
26. april 2022
Studieafslutning (Faktiske)
31. maj 2022
Datoer for studieregistrering
Først indsendt
26. marts 2021
Først indsendt, der opfyldte QC-kriterier
26. marts 2021
Først opslået (Faktiske)
30. marts 2021
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
20. juli 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. juli 2022
Sidst verificeret
1. juli 2022
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- IPRHO-KOREHAB2021
Plan for individuelle deltagerdata (IPD)
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