- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07609459
Study Protocol: The Jerte Valley as an Inclusive Outdoor Classroom. Smart and Active Tourism.
19 maj 2026 uppdaterad 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.
Studieöversikt
Status
Har inte rekryterat ännu
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Beräknad)
35
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Noelia Mayordomo-Pinilla, Master
- Telefonnummer: +34 569879797
- E-post: noeliamp@unex.es
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Barn
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Ja
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Övrig
- Tilldelning: Randomiserad
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: 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.
|
|
Övrig: 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.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Perception of accesibility (Physical and Social Accessibility Scale)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Beräknad)
1 juni 2026
Primärt slutförande (Beräknad)
1 juli 2026
Avslutad studie (Beräknad)
1 augusti 2026
Studieregistreringsdatum
Först inskickad
6 maj 2026
Först inskickad som uppfyllde QC-kriterierna
19 maj 2026
Första postat (Faktisk)
27 maj 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
27 maj 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
19 maj 2026
Senast verifierad
1 maj 2026
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- UdeExtremadura
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
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