Investigation of the Effects of Angling as Supportive Therapy in Schizophrenia Treatment on Serum Parameters, Anxiety, Depression, and Quality of Life
Angling as a Supportive Therapy in the Treatment of Schizophrenia
1 other identifier
interventional
60
1 country
1
Brief Summary
This study aims to evaluate the effects of recreational fishing (angling) as a supportive therapeutic intervention in individuals diagnosed with schizophrenia. Schizophrenia is a chronic psychiatric disorder characterized by disturbances in thinking, perception, emotion, and behavior, often accompanied by negative symptoms such as social withdrawal, anhedonia, and cognitive impairment, which significantly reduce quality of life. Recreational activities, particularly those involving nature-based engagement, have been shown to support psychological well-being through stress reduction, improved attention, and enhanced mood regulation. Angling is considered a mindfulness-like recreational activity that promotes relaxation, concentration, and emotional regulation, potentially offering benefits for individuals with psychiatric conditions. In this randomized controlled study, participants with schizophrenia will engage in a structured recreational fishing program in addition to standard care. The effects of the intervention will be evaluated on biochemical serum parameters, anxiety and depression levels, and quality of life outcomes. The study also aims to assess the psychosocial well-being of participants and determine the feasibility of integrating angling as an adjunctive non-pharmacological intervention in schizophrenia care. The findings are expected to contribute to evidence-based complementary treatment approaches in psychiatric rehabilitation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 15, 2026
CompletedFirst Submitted
Initial submission to the registry
June 26, 2026
CompletedFirst Posted
Study publicly available on registry
July 6, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 15, 2026
ExpectedJuly 7, 2026
July 1, 2026
1 month
June 26, 2026
July 2, 2026
Conditions
Outcome Measures
Primary Outcomes (6)
The Positive and Negative Syndrome Scale
The Positive and Negative Syndrome Scale : he Positive and Negative Syndrome Scale (PANSS), developed by Kay et al., is a semi-structured clinician-rated instrument consisting of 30 items scored on a 7-point scale (1 = absent to 7 = extreme). The scale comprises three subscales: positive symptoms (7 items; score range: 7-49), negative symptoms (7 items; score range: 7-49), and general psychopathology (16 items; score range: 16-112). Total PANSS scores range from 30 to 210, with higher scores indicating more severe psychopathology and poorer clinical status.
Baseline and immediately after the 8-week intervention.
Quality of Life Scale for Schizophrenia Patients
Developed by Heinrich et al. to assess the quality of life of schizophrenia patients, the Turkish validity and reliability study was conducted by Soygür et al. Administered in a semi-structured interview format, the scale evaluates the individual's symptoms and level of functioning over the past four weeks. It consists of 21 items and four sub-dimensions: interpersonal relationships, occupational role, mental symptoms, and daily activities. Scores on the scale range from 0 to 126, with higher scores indicating better quality of life.
Baseline and immediately after the 8-week intervention.
UCLA Loneliness Scale
The UCLA Loneliness Scale-Short Form (ULS-8) is an 8-item self-report instrument used to assess perceived loneliness. Each item is rated on a 4-point Likert scale ranging from 1 ("Never") to 4 ("Always"). Two items are reverse scored. Total scores range from 8 to 32, with higher scores indicating greater perceived loneliness.
Baseline and immediately after the 8-week intervention.
Serum Beta-Endorphin Concentration
Venous blood samples will be collected to measure serum beta-endorphin concentration. Changes in serum beta-endorphin levels will be evaluated to assess the biological effects of the intervention.
Baseline and immediately after the 8-week intervention.
Serum Serotonin Concentration
Venous blood samples will be collected to measure serum serotonin concentration. Changes in serum serotonin levels will be evaluated to assess the biological effects of the intervention.
Baseline and immediately after the 8-week intervention.
Serum Cortisol Concentration
Venous blood samples will be collected to measure serum cortisol concentration. Changes in serum cortisol levels will be evaluated to assess the biological effects of the intervention.
Baseline and immediately after the 8-week intervention.
Study Arms (2)
recreational fishing (angling)
EXPERIMENTALControl
NO INTERVENTIONInterventions
Eligibility Criteria
You may qualify if:
- Adults aged 18 years and older
- Able to communicate verbally
- Diagnosed with schizophrenia
- Able to provide written informed consent
You may not qualify if:
- Presence of comorbid psychiatric disorders other than schizophrenia
- Patients in the acute psychotic (attack) phase
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Firat Universitylead
Study Sites (1)
Fırat university
Elâzığ, Center, 25240, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 26, 2026
First Posted
July 6, 2026
Study Start
June 15, 2026
Primary Completion
July 15, 2026
Study Completion (Estimated)
August 15, 2026
Last Updated
July 7, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share