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Early Mindfulness Based Cognitive Therapy for Prevention of Psychological Distress in Cancer Patients

Early Mindfulness Based Cognitive Therapy for Prevention of Psychological Distress in Cancer Patients

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07124481
Acronym
EarlyMind
Enrollment
208
Registered
2025-08-15
Start date
2025-10-31
Completion date
2027-10-31
Last updated
2025-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Mindfulness Based Cognitive Therapy

Brief summary

The goal of this clinical trial is to learn if early provision of mindfulness based cognitive therapy can prevent psychological distress in adult patients with cancer one year after diagnosis. Researchers will compare mindfulness based cognitive therapy to usual care to see if psychological distress is lower in patients that followed mindfulness. Participants will follow 8 weekly sessions of mindfulness and fill in questionnaires.

Interventions

BEHAVIORALMindfulness based stress reduction

8 weekly sessions of 2.5 hour per session, face-to-face in a group consisting of maximum 15 participants, supervised by a certified mindfulness trainer

Sponsors

Helen Dowling Institute
CollaboratorUNKNOWN
Isala
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with urological cancer or breast cancer * \<6 weeks since cancer diagnosis * Planned curative treatment or palliative treatment with life expectation \>1 year * Good proficiency in Dutch language

Exclusion criteria

* Serious psychiatric history or current psychiatric treatment (interfering with study participation): 1) current suicidal ideation, 2) current psychosis or bipolar disorder, 3) psychosis or bipolar disorder in history * Unable to understand study procedure * A priori unable to be available for 8 week MBCT

Design outcomes

Primary

MeasureTime frameDescription
Psychological distressFrom enrollment to 2 years after diagnosisAnxiety and depression as measured with the Hospital Anxiety and Depression Scale

Contacts

Primary ContactMarit Mentink, PhD
m.d.c.mentink@isala.nl+31657643188
Backup ContactEva Noorda, PhD
evanoorda@gmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026