- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07609459
Study Protocol: The Jerte Valley as an Inclusive Outdoor Classroom. Smart and Active Tourism.
19. mai 2026 oppdatert av: Noelia Mayordomo, Universidad de Extremadura
To promote the inclusion of people with disabilities, an outdoor intervention will be conducted involving physical activities with adolescents with and without disabilities.
The study will be designed as a randomized controlled trial (RCT) with a control group that will not participate in these activities, and will include three time points (pre-intervention, post-intervention, and follow-up).
The study will assess sociodemographic, accessibility, socio-emotional, and group cohesion variables.
Studieoversikt
Status
Har ikke rekruttert ennå
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
35
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Noelia Mayordomo-Pinilla, Master
- Telefonnummer: +34 569879797
- E-post: noeliamp@unex.es
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Ja
Beskrivelse
Inclusion Criteria:
- 12 -16 years
- Enrollment in public schools and special education centers
- Informed consent signed by tutors
Exclusion Criteria:
- Have health issues that prevent them from participating in physical activity or pose a safety risk to participants
- Not having a signed informed consent
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Randomisert
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Active tourism
Participants in the experimental group will attend an informational session on disability and take part in an interactive workshop where they will experience the challenges and sensations faced by people with disabilities to empathize with them and understand their reality.Subsequent to this workshop, participants will engage in a series of activities, beginning with whitewater rafting, followed by canyoning, and concluding with kayaking.
These activities are designed to be inclusive, accommodating individuals both with and without disabilities.
Following workshops and activities based on smart and active tourism, the personal experiences of people with and without disabilities will be shared, fostering a dialogue that further enhances the understanding of the reality faced by people with functional diversity.
|
Participants in the experimental group will attend an informational session on disability and take part in an interactive workshop where they will experience the challenges and sensations faced by people with disabilities to empathize with them and understand their reality.Subsequent to this workshop, participants will engage in a series of activities, beginning with whitewater rafting, followed by canyoning, and concluding with kayaking.
These activities are designed to be inclusive, accommodating individuals both with and without disabilities.
Following workshops and activities based on smart and active tourism, the personal experiences of people with and without disabilities will be shared, fostering a dialogue that further enhances the understanding of the reality faced by people with functional diversity.
|
|
Annen: Divulgation, not intervention
Students will participate in a workshop on disability awareness.
The workshop will be the same for this group and the group participating in outdoor physical activities.
During the workshop, students will learn about disabilities and experience a simulation using eye masks and tongue depressors to simulate visual and speech impairments.
|
: Students will participate in a workshop on disability awareness.
The workshop will be the same for this group and the group participating in outdoor physical activities.
During the workshop, students will learn about disabilities and experience a simulation using eye masks and tongue depressors to simulate visual and speech impairments.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Perception of accesibility (Physical and Social Accessibility Scale)
Tidsramme: Through study completion, an average of one month
|
This scale measures perceptions of accessibility in one's environment, focusing on physical and social aspects and considering how social interactions and inclusion influence daily life.
A Likert scale ranging from 1 ( "extremely inaccessible") to 5 ( "extremely accessible ") was used to measure these perceptions.
|
Through study completion, an average of one month
|
|
Perception of group cohesion (Group Environment Questionnaire)
Tidsramme: Through study completion, average of 1 month
|
Assesses the perceptions of group cohesion.
This questionnaire includes factors related to personal attraction to group tasks, personal motivation toward the social group, engagement in group tasks, and group-social unity.
|
Through study completion, average of 1 month
|
|
Perception of attitudes towards inclusion (AISDPE)
Tidsramme: Through study completion, an average of one month follow up
|
This scale consists of 17 items divided into two dimensions: cognitive perception (seven items) and behavioral intention (ten items).
The scores were determined using a Likert scale ranging from 1 ("strongly disagree") to 5 ("strongly agree").
|
Through study completion, an average of one month follow up
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
1. juni 2026
Primær fullføring (Antatt)
1. juli 2026
Studiet fullført (Antatt)
1. august 2026
Datoer for studieregistrering
Først innsendt
6. mai 2026
Først innsendt som oppfylte QC-kriteriene
19. mai 2026
Først lagt ut (Faktiske)
27. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
27. mai 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
19. mai 2026
Sist bekreftet
1. mai 2026
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- UdeExtremadura
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
UBESLUTTE
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