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Search / Trial NCT06766526

Internet-based Support for Adjustment to Prostate Cancer

Launched by LINKOEPING UNIVERSITY · Jan 8, 2025

Trial Information

Current as of August 20, 2025

Recruiting

Keywords

Psychological Distress Prostate Cancer Cancer Icbt Cognitive Behavior Therapy

ClinConnect Summary

This clinical trial is exploring how effective internet-based cognitive behavior therapy (ICBT) can be in helping men who have been diagnosed with prostate cancer manage feelings of distress, anxiety, and depression. The study is looking for men aged 18 and older who have experienced psychological symptoms after their prostate cancer diagnosis and who are not currently undergoing medical treatment. Participants will be randomly assigned to either receive an eight-week tailored ICBT program, which includes weekly support from a trained therapist, or to a control group that also receives therapist support but without the specific ICBT focus.

To be eligible, participants should have a certain level of psychological distress, as measured by a specific questionnaire. They must be able to communicate in Swedish and have access to a computer or smartphone with the internet. Importantly, men who have recently undergone treatment for prostate cancer or who have severe mental health issues that might affect their ability to participate will not be included in the study. This trial is currently recruiting participants, and it offers a supportive way for men dealing with prostate cancer to improve their mental well-being from the comfort of their homes.

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • Subjectively reported psychological symptoms and problems that have come about after a prostate cancer diagnosis.
  • A sum score above 19 on the primary outcome measure (Kessler-10).
  • An age of 18 or older.
  • Ability to speak, read, and write Swedish.
  • Access to a computer/laptop/tablet/smartphone and internet access.
  • Sufficient computer profiency to be able to use the treatment platform.
  • Exclusion Criteria:
  • Planned medical treatment or planned change in medication related to the prostate cancer during the treatment period.
  • Recently finished (within the past six months) medical treatment for prostate cancer.
  • Severe psychiatric or somatic conditions that impedes participation in the study.
  • Ongoing substance use problems.
  • Acute suicidality.
  • Other ongoing psychological treatment.
  • Psychopharmaceutic treatment that has been changed within the past month or with planned changes during the treatment phase.

About Linkoeping University

Linköping University is a leading academic institution in Sweden, renowned for its innovative research and commitment to advancing medical science. With a strong emphasis on interdisciplinary collaboration, the university facilitates cutting-edge clinical trials aimed at improving patient outcomes and enhancing healthcare delivery. Linköping University’s research initiatives are supported by state-of-the-art facilities and a robust network of partnerships with healthcare providers, industry stakeholders, and regulatory bodies, ensuring rigorous methodologies and ethical standards in all clinical investigations. Through its dedication to research excellence, Linköping University plays a pivotal role in translating scientific discoveries into practical applications that benefit society.

Locations

Linköping, , Sweden

Patients applied

0 patients applied

Trial Officials

Gerhard Andersson, pHD

Principal Investigator

Linkoeping University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported