NCT07682935

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
0mo left

Started Jun 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress77%
Jun 2026Aug 2026

Study Start

First participant enrolled

June 15, 2026

Completed
11 days until next milestone

First Submitted

Initial submission to the registry

June 26, 2026

Completed
10 days until next milestone

First Posted

Study publicly available on registry

July 6, 2026

Completed
9 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 15, 2026

Expected
Last Updated

July 7, 2026

Status Verified

July 1, 2026

Enrollment Period

1 month

First QC Date

June 26, 2026

Last Update Submit

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)

EXPERIMENTAL
Behavioral: recreational fishing (angling)

Control

NO INTERVENTION

Interventions

Fishing will be done.

recreational fishing (angling)

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Study Sites (1)

Fırat university

Elâzığ, Center, 25240, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Schizophrenia

Condition Hierarchy (Ancestors)

Schizophrenia Spectrum and Other Psychotic DisordersMental Disorders

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

Locations