Acceptance and Commitment Therapy (ACT-HBC) for the Improvement of Cancer Distress in Patients With Hepatobiliary Cancers

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMayo Clinic

About this trial

This clinical trial studies whether Acceptance and Commitment Therapy for patients with hepatobiliary cancers (ACT-HBC) can be used to help improve cancer distress. Patients with hepatobiliary cancer (HBC) often experience high levels of distress and reductions in quality of life. ACT-HBC is a behavioral intervention tailored to patients with HBC. It helps patients cope with difficult thoughts and emotions while staying connected to what matters most in life, which may be an effective way to improve cancer distress.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

HBC diagnosis

Age >= 18 years

Able to provide written informed consent

Verbally endorse cancer distress

Disqualifiers

Other psychological therapy that started =< 2 months prior to prospective enrollment

Inability to actively participate in and learn from group therapy (e.g., active/uncontrolled psychotic symptoms, neurological condition, personality pathology) as determined by clinical judgement in Behavioral Medicine Program (BMP) consultation. Individual therapy or alternative group therapy will be offered to patients ineligible per this criterion

HBC remission

Trial design

Design model

Single group

Treatments tested in this trial

  • Acceptance and Commitment Therapy

    Behavioral

    Attend ACT-HBC telehealth group sessions

  • Questionnaire Administration

    Other intervention

    Ancillary studies

  • Telemedicine

    Other intervention

    Attend ACT-HBC telehealth group sessions

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Supportive care (ACT-HBC)Experimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Patient satisfaction

The Institute for Healthcare Improvement 10-point Likert scale (0-10) asks: "Would you recommend this program to your friends and family?" A score ≥ 7 indicates high individual satisfaction. Program satisfaction is achieved if 50% of individuals meet this cut-off.

Time frame
At 8 weeks
2

Patient session attendance (Feasibility)

Feasibility will be determined by the number of patients attending ≥ 4 sessions.

Time frame
At 8 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.