An ecological momentary compassion-focused intervention for enhancing resilience in help-seeking youths

Withdrawn

Conditions: angst en depressieve symptomen
psychotic symptoms
psychotic-like experiences
10039628

Registration Number: NL-OMON45680

Lead Sponsor: Mondriaan Zorggroep (Heerlen)

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Withdrawn

Sex: Not specified

Target Recruitment: 150

Inclusion Criteria

1. Age from 15 until 26 years
2. Score of 6 or above on the PQ, a T-score of 63 or above on the BSI, and/or a score above the cutoff on the SQ-48 (i.e., on the social phobia (>9), depression (>8), or anxiety (>11) subscale)
3. Willingness to participate in the compassion-focused ecological momentary intervention
4. Ability to give written informed consent independently

Exclusion Criteria

1. Insufficient command of Dutch so that the compassioned-focused ecological momentary intervention cannot be followed and outcomes cannot be reasonably assessed in Dutch
2. Clinical diagnosis of alcohol or substance dependency, severe endocrine, cardiovascular or organic brain disease

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Stress sensitivity, psychotic, anxiety and depressive symptoms measured with<br /><br>Ecological Momentary Assessment (EMA) and other validated measures will be the<br /><br>primary outcomes, which will be obtained before randomization (baseline), at<br /><br>the end of the 3-week intervention period (post-intervention), and after a<br /><br>4-week and 10-week follow-up period (follow-up). Our primary hypothesis<br /><br>relates to endpoints at the end of treatment.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The secondary study parameters will be threat anticipation, appraisal of<br /><br>emotions, interpersonal sensitivity, and general psychopathology, measured with<br /><br>EMA and other validated measures. As the primary outcomes, secondary outcomes<br /><br>will be obtained before randomization (baseline), at the end of the 3-week<br /><br>intervention period (post-intervention), and after a 4-week and 10 week<br /><br>follow-up period (follow-up).</p><br>