CBT on Fatigue in Survivors of Hodgkin Lymphoma
Cognitive Behavioral Therapy (CBT) Web-based Intervention on Fatigue in Survivors of Hodgkin Lymphoma - a Pilot Study
Background: Cancer-related fatigue is one of the most common patient-reported impairments in survivors of Hodgkin lymphoma and is associated with adverse effects on psychological well-being and everyday life including family, work and social participation.
Methods: The investigators here present a bi-centric (Cologne and Leipzig) pilot-study for a web-based intervention (Cognitive Behavioral Therapy) on cancer-related fatigue. In detail, the investigators will conduct a non-randomized and non-controlled before-and-after study in a minimum of 20 survivors of Hodgkin lymphoma. Levels of fatigue and quality of life will be measured before the intervention (T0), post-intervention (T1) and at 3-months follow-up (T2).
Results: The investigators will provide information regarding the feasibility of the intervention (i.e., response rate, patient and therapist adherence, and patient satisfaction) and preliminary results on the efficacy of the program in reducing CRF and increasing levels of quality of life.
Aims: The results of this pilot-study will provide essential information to conduct a future randomized clinical trial to investigate the efficacy of this intervention in reducing cancer-related fatigue in survivors with Hodgkin lymphoma.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
Concrete Aims: The investigators aim to conduct a a feasibility study, e.g., a pilot study before a randomized controlled trial can be planned in detail. This initial pilot-study is intended to test out the standard operating procedures, evaluate the feasibility, acceptance and adherence to the study protocol as well as preliminary efficacy of the web-based intervention for survivors of Hodgkin lymphoma. In detail, this study contains all preparation for conducting a trial, i.e., the translation, the adaptation and evaluation of the cognitive-behavioral web-based intervention manual from the original Dutch Version, the adaptation and implementation of all necessary technical and research-administrative requirements to successfully conduct the web-based randomized controlled trial and the evidence-based training of all study therapists including the implementation of therapists supervision. The investigators further assess adherence of the patients and therapists, the response rate and the patient satisfaction. Furthermore, preliminary efficacy of the intervention will be tested assessing levels of fatigue and quality of life at each measurement point.
Study Design: The design of this pilot web-based intervention on treating fatigue will be a non-randomised prospective non-controlled before-and-after study, in which observations will be made only in a patient group that receives the intervention. No control group will be recruited. Assessments will be conducted on the three measurement points: before the therapy (T0), after the intervention (T1) and 3 months after the intervention (T2).
Intervention: The internet-based cognitive behavioral therapy on postcancer fatigue includes two face-to-face sessions with their therapist and eight web-based treatment modules, each approximately 45 minutes in length, delivered over 6 months. The intervention will be specifically tailored to the individual needs of each patient: The therapy model of cancer-related fatigue distinguishes six perpetuating factors: 1) insufficient processing of being diagnosed with Hodgkin lymphoma and being treated for it; 2) excessive fear of disease recurrence; 3) inactivity or a dysregulated (physical) activity pattern; 4) dysfunctional fatigue-related beliefs; 5) dysregulated sleep-wake pattern and 6) lack of social support. For each of these six cognitive-behavioural factors that can perpetuate fatigue a treatment module has been developed. The intervention will consist of a maximum of eight treatment modules: aside from the six modules addressing the fatigue maintaining factor there is a module on goal formulation and realization of goals.
Recruitment: the recruitment will be realized on the basis of two ongoing trials of the German Hodgkin study group (HD 16- HD18) where fatigue of the patients is measured continuously.
Duration: The duration for patients will be 9 months (6 months intervention, 3 month-follow-up assessment). The duration of the whole study will be 18 months.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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Cologne, Niemcy
- University Medical Center Cologne
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Saxony
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Leipzig, Saxony, Niemcy, 04103
- University Medical Center Leipzig
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- fluency in German language
- able to access the internet and use and follow a web-based Cognitive Behavioral intervention
- in complete remission after treatment for newly diagnosed HL without signs of relapse (no previous relapse)
- clinically relevant fatigue symptoms enduring at least 12 months after end of treatment (QLQ-C30 FA-12 ≥ 30 over at least two time points within the previous assessments in the course of the GHSG-trials)
- fatigue being related to HL and its treatment and interferes with usual functioning, i.e. fulfills the definition of CRF [1, 16].
Exclusion Criteria:
- Major communication difficulties
- severe cognitive impairment that would interfere with a patient's ability to give informed consent for research (indicated by the medical care team)
- Karnofsky Performance Status scale score < 70 predicting an expected survival of less than 6 months
- somatic co-morbidities that could explain the presence of severe fatigue (e.g. Chronic Obstructive Pulmonary Disease or heart failure) according to the hemato-oncologists examining the potential participant before inclusion for the study
- history of relapsed or refractory HL
- clinical symptoms which may indicate a relapse of HL
- current depressive disorder and related psychotropic or psychological treatment
- Currently receiving medical and/or psychological treatment for a psychiatric disorder, other than the use of an anti-depressant
- current treatment aimed at fatigue
- previous attempt to treat fatigue with behavioral psychological therapy
- pregnant or breastfeeding women
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie podtrzymujące
- Przydział: Nie dotyczy
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Cognitive Behavioral Therapy for Treating Fatigue
This is the patient group that receives the intervention (IG), i.e., the cognitive behavioral therapy for reducing fatigue.
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The internet-based CBT postcancer fatigue intervention includes two face-to-face sessions with their therapist and eight web-based treatment modules, each approximately 45 minutes in length, delivered over 6 months. The intervention will be specifically tailored to the individual needs of each patient: The CBT model of cancer-related fatigue distinguishes six perpetuating factors: 1) insufficient processing of being diagnosed with HL and being treated for it; 2) excessive fear of disease recurrence; 3) inactivity or a dysregulated (physical) activity pattern; 4) dysfunctional fatigue-related beliefs; 5) dysregulated sleep-wake pattern and 6) lack of social support. For each of these six cognitive-behavioural factors that can perpetuate fatigue a treatment module has been developed. |
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Odsetek odpowiedzi
Ramy czasowe: Okres oceny tego wyniku będzie trwał od rozpoczęcia rekrutacji do włączenia ostatniego pacjenta, co będzie wynosić około 1 roku.
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Badacze ocenią liczbę kwalifikujących się pacjentów, którzy chcą wziąć udział w badaniu, w stosunku do liczby pacjentów zaproszonych do udziału.
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Okres oceny tego wyniku będzie trwał od rozpoczęcia rekrutacji do włączenia ostatniego pacjenta, co będzie wynosić około 1 roku.
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Przestrzeganie zaleceń przez pacjenta
Ramy czasowe: Podczas fazy interwencji dla każdego pacjenta, która będzie trwała około 6 miesięcy.
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Przestrzeganie zaleceń przez pacjentów będzie oceniane na podstawie dokumentacji rezygnacji pacjentów.
Szczegółowo udokumentujemy, czy pacjenci opuszczą badanie w trakcie leczenia (a jeśli tak, to na jakim etapie).
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Podczas fazy interwencji dla każdego pacjenta, która będzie trwała około 6 miesięcy.
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Zadowolenie pacjenta
Ramy czasowe: Oceniane tylko raz dla każdego pacjenta, bezpośrednio po zakończeniu przez pacjenta interwencji.
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Oceniane za pomocą kwestionariusza (Inwentarz Sojuszu Roboczego – skrócony formularz poprawiony).
Przedstawiony zostanie łączny wynik w 12 pozycjach, oceniony na pięciostopniowej skali Likerta (w zakresie od 12 do 60).
Wyższe wartości oznaczają większą satysfakcję.
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Oceniane tylko raz dla każdego pacjenta, bezpośrednio po zakończeniu przez pacjenta interwencji.
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Therapist adherence
Ramy czasowe: Assessed during the intervention phase for each patient, i.e., within about 6 six months.
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Using information of the therapy protocols of each participant, it will be assessed if the treatment sessions were done according to the treatment protocol.
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Assessed during the intervention phase for each patient, i.e., within about 6 six months.
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Levels of fatigue 1
Ramy czasowe: Assessed at three time points: before the intervention, immediately after the intervention and 3 months after the intervention
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Assessed by a questionnaire, the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Module Measuring Cancer-Related Fatigue (EORTC QLQ-FA12).
The questionnaire assesses the level of cancer-related fatigue.
The sum score across all 12 items, rated on a 4-point Likert scale, will be reported (total range: 12-48).
Higher values indicate higher levels of fatigue (i.e., higher values indicate a worse outcome).
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Assessed at three time points: before the intervention, immediately after the intervention and 3 months after the intervention
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Levels of fatigue 2
Ramy czasowe: Assessed at three time points: before the intervention, immediately after the intervention and 3 months after the intervention
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Levels of fatigue will additionally assessed by a second questionnaire, the Checklist Individual Strength - Subscale Fatigue Severity.
The scale assesses the level of cancer-related fatigue.
The sum score across all 8 items, rated on a 7-point Likert scale, will be presented (total range: 8 - 56).
Higher values indicate higher levels of fatigue (i.e., higher values indicate a worse outcome).
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Assessed at three time points: before the intervention, immediately after the intervention and 3 months after the intervention
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Global quality of life
Ramy czasowe: Assessed at three time points: before the intervention, immediately after the intervention and 3 months after the intervention
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Global quality of Life will be assessed by the European Organisation for Research and Treatment of Cancer (EORTC), Quality of Life-questionnaire (EORTC QLQ-C30).
Global quality of life is assessed in a 2-item subscale of the questionnaire, each rated on a 7-point-Likert scale (total range: 2-14).
According to the questionnaire manual, however, the sum score of the two items will be linear-transformed to a 0-100 scale, with higher values indicating higher levels of quality of life (i.e., higher values indicate a better outcome).
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Assessed at three time points: before the intervention, immediately after the intervention and 3 months after the intervention
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Współpracownicy i badacze
Sponsor
Współpracownicy
Śledczy
- Główny śledczy: Anja Mehnert, Prof. Dr., University of Leipzig
- Główny śledczy: Peter Borchmann, Prof. Dr., University of Cologne
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 933 000-146
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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