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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03935243
Other study ID # 2019-STABLE
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 10, 2019
Est. completion date July 2020

Study information

Verified date December 2019
Source University of Zurich
Contact Nathalie Brackmann, Dr. phil.
Phone +41 (0)52 304 93 01
Email nathalie.brackmann@puk.zh.ch
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main object of this study is to evaluate the efficacy of equine assisted therapy on substantial and so far unsatisfactorily treatable symptom complexes in patients with schizophrenia.


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
equine assisted therapy
The equine assisted group therapy is carried out by a riding therapist (nurse psychiatry HF, certified riding therapist SG-TR). There is a detailed plan for the PT.
activating control phase
The control phase includes a generally activating employment offer, such as board games, light physical activations, roundtables and artistic design.

Locations

Country Name City State
Switzerland Psychiatrische Universitätsklinik Zürich Zürich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

References & Publications (21)

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Outcome

Type Measure Description Time frame Safety issue
Primary Changed negative symptoms retrieved from psychometric instruments (BNSS) after the intervention BNSS: 5 domains for the negative symptoms are recorded, namely "blunted affect", "alogie", "asociality", "anhedonia" and "avolition". The BNSS also distinguishes between the anticipatory and the consumptive aspects of anhedonia, which are distinct advantages over other questionnaires such as PANSS or SANS (Kirkpatrick 2011, Marder & Kirkpatrick 2014). With its 13 items that can be collected within 15 minutes, the BNSS is a short scale that, despite its shortness, has excellent inter-rater and test-retest reliability and good validity. Furthermore, there are only small correlations of the BNSS with masses of positive symptoms, anxiety and depression (Strauss et al., 2012, Kirkpatrick et al., 2011). Like the PSP scale, the BNSS is surveyed during the first, second and third rounds and here too the surveys are conducted by experienced psychologists or psychiatrists. week 0 (t1), week 8 +/- 1 day (t2), week 15 +/- 2 days (t3)
Primary Changed psychosocial functioning after the intervention (PSP) PSP: External rating scale consisting of 4 subscales, which are calculated to a total score ranging from 0 to 100. The 4 scales are "disturbing and aggressive behavior," "self-care," "socially beneficial activities," and "personal and social relationships" (Morosini et al., 2000). The individual items are queried on a 6-point scale, which includes the expressions "absent", "easy", "obvious", "pronounced", "severe" and "extremely serious". Explanations are available for the respective characteristics. Schaub and Juckel (2011) have also created an interview guide for the German version, which should further simplify the assessment. The individual surveys are carried out by experienced psychologists or psychiatrists. The PSP scale was chosen because it is quick and easy to query, has a higher information content than other scales (e.g., SOFAS or GAF), and also has high validity and reliability. week 0 (t1), week 8 +/- 1 day (t2), week 15 +/- 2 days (t3)
Secondary Changed quality of life (Quality of Life Questionnaire in Schizophrenia (S-QoL) This is done using the standardized method S-QoL (Auquier et al., 2003). It uses 41 items to record 8 subscales of the quality of life such as well-being, self-esteem, resilience and autonomy. The S-QoL is a self-assessment tool and its application takes 15 minutes. week 0 (t1), week 8 +/- 1 day (t2), week 15 +/- 2 days (t3)
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