Internet-delivered CBT for NCCP-patients - a Pilot Trial

Linkoeping University15 enrolled

Overview

This pilot randomized controlled trial (RCT) aims to test the feasibility and effectiveness of a guided internet-delivered cognitive behavioural therapy intervention in the treatment of cardiac anxiety and fear of body sensations in patients with non-cardiac chest pain. The control group will receive care-as-usual.

Despite reassurance, many patients with non-cardiac chest pain (NCCP) think they have an undetected cardiac disease and avoid activities that they think might be harmful to their heart. These patients need help and support to evaluate the way they perceive and handle their chest pain. Therefore, we have developed a 4 session guided intervention based on cognitive behavioural therapy that will be delivered via internet. The intervention consists of psychoeducation, exposure to physical activity, and a breathing-based relaxation exercise. The goal with the intervention is to help the participants modify their beliefs about chest pain, change their cognitive and behavioural strategies, and give them tools to handle chest pain to prevent them from relapse.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Chest Pain Anxiety Fear

Interventions

Internet-delivered cognitive behavioural therapyBEHAVIORAL

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * recurrent chest pain that has been diagnosed as non-cardiac at least twice during last 6 months * patients screened positive for avoidance of physical activity due to cardiac anxiety and/or fear of body sensations Exclusion Criteria: * no regular access to a computer/tablet computer with internet connection * language difficulties * not able to perform physical activity/exercise test due to physical constraints * patients with severe depressive symptoms * patients with acute ischemic heart disease

Locations (1)

Linkoeping University

Linköping, Sweden

Outcomes

Primary Outcomes

Cardiac anxiety (Data collection)

Data collection will be performed before and after the intervention, and 3 and 12 months after the end of the intervention

Time frame: 12 months

Secondary Outcomes

Fear of body sensations (Data collection)

Data collection will be performed before and after the intervention, and 3 and 12 months after the end of the intervention

Time frame: 12 months

Depressive symptoms (Data collection)

Data collection will be performed before and after the intervention, and 3 and 12 months after the end of the intervention

Time frame: 12 months

Healthcare utilization and costs (Data collection)

Data collection will be performed12 months after the end of the intervention

Time frame: 12 months

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.