- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT04822389
Telerehabilitation and Lymphoma Patients
19 juli 2022 uppdaterad av: 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.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Interventionell
Inskrivning (Faktisk)
15
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
-
Brno, Tjeckien, 62500
- University Hospital Brno
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Stödjande vård
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: 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.
|
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.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Cardiorespiratory fitness (CRF)
Tidsram: Change from baseline to 12 weeks and 1-year
|
Peak oxygen uptake (VO2peak) during the cardiopulmonary exercise test
|
Change from baseline to 12 weeks and 1-year
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Body composition (Total muscle mass in kilograms)
Tidsram: Change from baseline to 12 weeks and 1-year
|
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.
|
Change from baseline to 12 weeks and 1-year
|
|
Body composition (Body fat mass in kilograms)
Tidsram: Change from baseline to 12 weeks and 1-year
|
Body fat mass is the actual weight of fat in body.
Body fat mass will be measured by bioelectrical impedance analysis.
|
Change from baseline to 12 weeks and 1-year
|
|
Body composition (Body weight in kilograms)
Tidsram: Change from baseline to 12 weeks and 1-year
|
Body weight is the measurement of weight without items located on the person.
Body weight will be measured by bioelectrical impedance analysis.
|
Change from baseline to 12 weeks and 1-year
|
|
Incidence of treatment-emergent adverse events assessed by 5 grade scale
Tidsram: Data will be recorded continuously from the baseline to 12 weeks
|
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
|
Data will be recorded continuously from the baseline to 12 weeks
|
|
Exercise adherence
Tidsram: 12 weeks
|
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.
|
12 weeks
|
|
Exercise compliance
Tidsram: 12 weeks
|
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)
|
12 weeks
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
1 april 2021
Primärt slutförande (Faktisk)
26 april 2022
Avslutad studie (Faktisk)
31 maj 2022
Studieregistreringsdatum
Först inskickad
26 mars 2021
Först inskickad som uppfyllde QC-kriterierna
26 mars 2021
Första postat (Faktisk)
30 mars 2021
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
20 juli 2022
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
19 juli 2022
Senast verifierad
1 juli 2022
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- IPRHO-KOREHAB2021
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .