Cognitive Behavioral Therapy for Insomnia for Cancer-Related Fatigue

AM
MS
Overseen ByMark Seewald
Age: 18+
Sex: Female
Trial Phase: Academic
Sponsor: Abramson Cancer Center at Penn Medicine
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Approved in 3 JurisdictionsThis treatment is already approved in other countries

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests whether varying amounts of Cognitive Behavioral Therapy for Insomnia (CBT-I) can reduce cancer-related fatigue. Many cancer patients face both fatigue and insomnia, which can diminish their quality of life. The study divides participants into groups, each receiving a different number of CBT-I sessions to determine the most effective approach. Suitable candidates have undergone radiation treatment for bladder cancer and experience both insomnia and cancer-related fatigue. As an unphased trial, this study provides a unique opportunity to explore personalized treatment options for enhancing quality of life.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that Cognitive Behavioral Therapy for Insomnia (CBT-I) is generally safe and well-tolerated. Studies have found that CBT-I can greatly improve sleep problems, especially for cancer survivors. This therapy not only helps with insomnia but also reduces fatigue, which is common in cancer patients.

Patients have experienced significant benefits from CBT-I without major side effects. Most people manage the therapy well, with few reports of negative effects. Overall, evidence suggests that CBT-I is a safe choice for treating insomnia and fatigue in cancer patients.12345

Why are researchers excited about this trial?

Researchers are excited about Cognitive Behavioral Therapy for Insomnia (CBT-I) as a treatment for cancer-related fatigue because it targets sleep issues directly, which can significantly impact fatigue levels. Unlike standard treatments that often involve medications to manage symptoms, CBT-I is a non-pharmacological approach that empowers patients with practical strategies to improve sleep quality. This therapy offers flexibility, with various session lengths (four, eight, ten, or twelve sessions), allowing for personalized treatment plans to meet individual needs. By addressing insomnia, CBT-I aims to enhance overall well-being and reduce fatigue, offering a promising alternative to traditional methods.

What evidence suggests that this trial's treatments could be effective for cancer-related fatigue?

Research has shown that Cognitive Behavioral Therapy for Insomnia (CBT-I) can reduce cancer-related tiredness. One study found that CBT-I greatly improved fatigue in cancer patients by enhancing sleep quality. Another study demonstrated that CBT-I significantly reduced the severity of insomnia. CBT-I also effectively treats cancer-related fatigue while managing other common health issues. For cancer survivors, online CBT-I with support provided significant relief from insomnia. Overall, CBT-I appears to be a promising method for improving both sleep and tiredness in cancer patients. Participants in this trial will receive varying numbers of CBT-I sessions to evaluate its effectiveness.26789

Are You a Good Fit for This Trial?

This trial is for breast cancer patients aged 25-85 who are experiencing both insomnia and cancer-related fatigue, without significant medical conditions like sleep apnea or psychiatric disorders. Participants must not have metastatic disease, untreated sleep apnea, a history of narcolepsy, substance dependence, or work night shifts.

Inclusion Criteria

I have significant issues with sleep and fatigue.
My breast cancer is limited to the breast.
I am currently undergoing or have completed radiation therapy.
See 2 more

Exclusion Criteria

History of narcolepsy
I have untreated sleep apnea or high scores on the STOP-BANG test.
I have not been diagnosed with breast cancer.
See 6 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive CBT-I sessions conducted weekly via Telehealth, with session numbers varying between four, eight, ten, or twelve based on randomization

4-12 weeks
Weekly sessions (virtual)

Follow-up

Participants are monitored for safety and effectiveness after treatment, including completion of questionnaires on sleep and fatigue

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Cognitive Behavioral Therapy for Insomnia
Trial Overview The study tests whether different doses of Cognitive Behavioral Therapy for Insomnia (CBT-I) can improve sleep duration and reduce fatigue in breast cancer patients. It aims to understand if adjusting the amount of CBT-I can lead to better quality of life and survivorship outcomes.
How Is the Trial Designed?
4Treatment groups
Experimental Treatment
Group I: Twelve Sessions of CBT-IExperimental Treatment1 Intervention
Group II: Ten Sessions of CBT-IExperimental Treatment1 Intervention
Group III: Four Sessions of CBT-IExperimental Treatment1 Intervention
Group IV: Eight Sessions of CBT-IExperimental Treatment1 Intervention

Cognitive Behavioral Therapy for Insomnia is already approved in United States, European Union, United Kingdom for the following indications:

🇺🇸
Approved in United States as CBT-I for:
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Approved in European Union as CBT-I for:
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Approved in United States as Somryst for:
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Approved in United Kingdom as Sleepio for:

Find a Clinic Near You

Who Is Running the Clinical Trial?

Abramson Cancer Center at Penn Medicine

Lead Sponsor

Trials
425
Recruited
464,000+

University of Pennsylvania

Lead Sponsor

Trials
2,118
Recruited
45,270,000+

Abramson Cancer Center of the University of Pennsylvania

Lead Sponsor

Trials
360
Recruited
108,000+

National Cancer Institute (NCI)

Collaborator

Trials
14,080
Recruited
41,180,000+

Published Research Related to This Trial

In a study involving 173 cancer outpatients, 57% reported significant insomnia symptoms, and 80% of those willing to participate found the video-based cognitive behavioral therapy for insomnia (VCBT-I) acceptable, indicating a strong demand for this intervention.
Participants experienced increased knowledge about sleep and improved sleep quality after using VCBT-I, although technical and contextual barriers were noted, suggesting that remote professional support could enhance the effectiveness and personalization of the therapy.
Feasibility of a video-based cognitive behavioral therapy for insomnia in French adult cancer outpatients: results from the Sleep-4-All-1 study.Boinon, D., Charles, C., Fasse, L., et al.[2021]
The study aims to evaluate the effectiveness of digital cognitive behavioral therapy for insomnia (dCBT-I) compared to sleep hygiene education (SHE) in 308 women with cancer experiencing insomnia, with assessments at 12 and 24 weeks.
The primary outcome will measure changes in sleep quality using the Sleep Condition Indicator (SCI) score, helping to determine if dCBT-I provides better management of insomnia than SHE in this population.
The Sleepio after cancer (SAC) study. Digital cognitive behavioural therapy for insomnia (dCBT-I) in women cancer patients - Trial protocol of a randomised controlled trial.Treacy, T., O'Meara, Y., Galligan, MC., et al.[2023]
Cognitive Behavioral Therapy for Insomnia (CBT-I) has been shown to significantly improve sleep quality and psychological outcomes in cancer patients and survivors, based on a review of 12 studies.
CBT-I not only enhances sleep but may also positively affect mood, fatigue, and overall quality of life, and it can be delivered through various methods to reach more patients.
Sleeping well with cancer: a systematic review of cognitive behavioral therapy for insomnia in cancer patients.Garland, SN., Johnson, JA., Savard, J., et al.[2022]

Citations

1.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/39987779/
Web-based cognitive-behavioral therapy for insomnia in ...Conclusions: Web-based CBT-I with clinician support appears to be an effective treatment for insomnia in cancer survivors, offering meaningful benefits for ...
Impact and mechanisms of cognitive behavioral therapy for ...CBT-I resulted in significant improvement in fatigue, and these effects were largely accounted for by changes in insomnia. CBT-I is a robust intervention with ...
Voice-Activated Cognitive Behavioral Therapy for InsomniaThis randomized clinical trial of an in-home, voice-activated CBT-I program among breast cancer survivors found that the intervention improved insomnia ...
4.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/40982264/
Cognitive Behavioral Therapy for Insomnia in People With ...CBT-I was associated with significantly improved outcomes for insomnia severity (g = 0.98; 95% CI, 0.81-1.16) and moderate effect sizes ...
Cognitive Behavioral Therapy-Insomnia Demonstrates ...Use of cognitive behavioral therapy for insomnia (CBT-I) was effective in treating cancer-related fatigue (CRF) while controlling for the common comorbidities.
Web-based cognitive-behavioral therapy for insomnia in ...Web-based CBT-I with clinician support appears to be an effective treatment for insomnia in cancer survivors, offering meaningful benefits for comorbid symptoms ...
Voice-Activated Cognitive Behavioral Therapy for InsomniaThis randomized clinical trial investigates whether in-home delivery of a daily voice-activated cognitive behavioral therapy program improves insomnia symptoms
Online Treatment of Cognitive Impairment and Insomnia in ...The investigators will conduct a randomized controlled trial of immediate treatment with CBT-I compared to a delayed treatment group with 124 cancer survivors ...
Effects of cognitive-behavioral therapy for insomnia compared ...Compared with controls, CBT-I improved insomnia at an average magnitude greater than half of the MIC but did not reach the MCID threshold.
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