Nature Photography for Mental Well-Being and Nature Connectedness in Young Adults
4 de setembro de 2026 atualizado por: Beijing Normal University
Nature Photography for Mental Well-Being and Nature Connectedness in Young Adults: A Randomized Controlled Trial
This study tests whether a nature photography intervention can improve mental well-being and nature connectedness in young adults with mild emotional distress, and examines self-compassion as a key mechanism in this process.
Participants are randomized to a nature photography group, a human-made object photography group , or a group receiving a stress management handbook.
Eight photography tasks are delivered through a mobile platform.
Outcomes are assessed at baseline, mid-intervention, post-intervention, and follow-up.
Visão geral do estudo
Status
Ainda não está recrutando
Descrição detalhada
This is a three-arm randomized controlled trial examining whether nature-based photography improves mental well-being and nature connectedness among young adults with mild emotional distress.
Participants are randomized to a nature photography intervention, an active control completing human-made object photography, or a control group receiving a stress management handbook.
The intervention runs for 16 days and comprises eight structured photography sessions.
The primary outcomes are depression (PHQ-9) and anxiety (GAD-7) symptoms at post-intervention.
Secondary outcomes include nature connectedness, self-compassion, positive and negative affect, meaning in life, and life satisfaction, assessed at baseline, mid-intervention, post-intervention, and one-month follow-up.
Changes in self-compassion, mindfulness, and nature connectedness are examined as hypothesized mechanisms of the intervention effect.
Tipo de estudo
Intervencional
Inscrição (Estimado)
300
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Contato de estudo
- Nome: Xue Weng
- Número de telefone: (86)0756-3683259
- E-mail: xueweng@bnu.edu.cn
Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Sim
Descrição
Inclusion Criteria:
- PHQ-9 score ≥ 5 or GAD-7 score ≥ 5 (presence of mild or greater emotional distress).
Exclusion Criteria:
- PHQ-9 score ≥20 or GAD-7 score ≥15 (severe depressive or anxiety symptoms).
- Currently receiving psychological counseling or psychiatric treatment.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Pesquisa de serviços de saúde
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: Nature-Based Photography Intervention
Nature-Based Photography
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Photography Participants complete an 8-session, 16-day nature-based photography intervention delivered through a WeChat mini-program (one session every two days).
Each session includes a guided photography theme focused on natural elements, mindfulness and self-compassion prompts, and expressive writing, followed by optional peer support (viewing, liking, and commenting on group members' photographs) and personalized AI-assisted supportive feedback at the end of the session.
The intervention is designed to improve mental well-being and strengthen nature connectedness through structured engagement with natural environments.
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Experimental: Human-Made Object Photography Intervention
Human-Made Object Photography
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Participants complete an 8-session, 16-day photography intervention delivered through a WeChat mini-program, matched to the intervention group on schedule and task structure, but photographing everyday human-made objects (e.g., study tools, architectural details, furniture).
Each session includes expressive writing; no nature-focused prompts, peer interaction, or AI-assisted feedback are provided.
This condition controls for photography behavior, app engagement, and task contact without the nature exposure or self-compassion components.
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Comparador Ativo: Brief Psychoeducational Stress Management Intervention
Brief Psychoeducational Stress Management
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Participants receive a self-guided digital stress management handbook over the 16-day intervention period, covering five structured modules: recognition of physical and emotional stress signals; structured energy and time management (goal decomposition, pomodoro technique, priority matrix); establishing healthy lifestyle routines (sleep hygiene, regular exercise, balanced diet); building interpersonal support networks; and accessing professional help and campus mental health resources.
Participants read the handbook at their own pace without photography tasks or interactive components.
This condition serves as an active comparator controlling for contact time and expectancy while excluding nature exposure and mindfulness-based self-compassion components.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Depressive Symptoms
Prazo: Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Depressive Symptoms Change in depressive symptoms measured by the Patient Health Questionnaire-9 (PHQ-9).The PHQ-9 consists of 9 items, with each item rated from 0 (not at all) to 3 (nearly every day).
Higher scores indicate greater severity of depressive symptoms and represent a worse outcome.
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Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Anxiety Symptoms
Prazo: Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Change in anxiety symptoms measured by the Generalized Anxiety Disorder-7 (GAD-7).The GAD-7 consists of 7 items, with each item rated from 0 (not at all) to 3 (nearly every day).Higher scores indicate greater severity of anxiety symptoms and represent a worse outcome.
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Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Nature Connectedness
Prazo: Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Change in connection with the natural environment measured by the Nature Connectedness Scale.
Higher scores indicate greater nature connectedness and represent a better outcome.
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Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Self-Compassion
Prazo: Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Change in self-compassion measured by the Self-Compassion Scale (SCS).
The scale rated on a 5-point Likert scale ranging from 1 (almost never) to 5 (almost always).
Higher scores indicate greater self-compassion and represent a better outcome.
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Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Positive and Negative Affect
Prazo: Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3)
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Change in emotional states measured by the Positive and Negative Affect Schedule (PANAS).The PANAS rated on a 5-point Likert scale ranging from 1 (very slightly or not at all) to 5 (extremely).
Higher Positive Affect scores indicate greater positive affect and represent a better outcome, whereas higher Negative Affect scores indicate greater negative affect and represent a worse outcome.
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Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3)
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Meaning in Life
Prazo: Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Change in perceived meaning and purpose in life measured by the Meaning in Life Questionnaire (MLQ).
The MLQ rated on a 7-point Likert scale ranging from 1 (absolutely untrue) to 7 (absolutely true).
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Baseline (T0), Post-intervention (T2, Day 16), and 1-month Follow-up (T3).
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Investigadores
- Diretor de estudo: xue weng, Study Principal Investigator, Beijing Normal University
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Estimado)
1 de setembro de 2026
Conclusão Primária (Estimado)
1 de dezembro de 2026
Conclusão do estudo (Estimado)
30 de abril de 2027
Datas de inscrição no estudo
Enviado pela primeira vez
31 de agosto de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
31 de agosto de 2026
Primeira postagem (Real)
3 de setembro de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
9 de setembro de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
4 de setembro de 2026
Última verificação
1 de setembro de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- Nature Photography
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
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