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GreenME Nature-based therapy evaluation, case 2 (Consorci Sanitari Maresme)

Advancing Greencare in Europe: an integrated multi-scalar approach for the expansion of nature-based therapies to improve Mental health Equity (GreenME). Nature-based therapy evaluation. Case 2 (Consorci Sanitari Maresme)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14970007
Enrollment
78
Registered
2025-05-16
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Treatment of high stress Mental and Behavioural Disorders

Interventions

Sponsors

Universitat Autònoma de Barcelona
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Between the ages of 18 – 75 years 2. Comply with eligibility criteria to access and take part on the evaluated intervention 3. Stress interference in daily life being significantly or very significantly (as assessed by the screening questionnaire) 4. Either: often or very often experiences of discrimination or prejudices in daily life OR Yes-experiencing persistent poor sleep quality/poor mood/low energy levels/sadness/fatigue/anxiety (as assessed by the screening questionnaire) 5. No previous (last month) or current participation in the same type of nature-based therapy we are evaluating

Exclusion criteria

Exclusion criteria: 1. Intellectual disability (ICD-11 6A00) 2. Phobias that can highly impact the capacity to benefit from our evaluated interventions, such as social and insect-related phobias (ICD-11 6B02, 6B03, 6B04) 3. Dissociative behaviours (ICD-11 6B60, 6B61, 6B62, 6B63, 6B64, 6B65, 6B66, 6E65, 6B6Y, 6B6Z) 4. Mental or behavioural symptoms, signs or clinical findings that can highly impact the capacity of the intervention group to benefit from our evaluated interventions or that increases their potential to become difficult cases to handle by guides (ICD-11 MB23.0, MB23.R, MB23.S)

Design outcomes

Primary

MeasureTime frame
At Screening/Baseline, 10 weeks (end of intervention), 14 weeks, and 22 weeks for the intervention group and at Screening/Baseline, 10 weeks, 20 weeks (end of intervention, for those who choose to enrol in the intervention after the initial waitlist period), and 24 weeks for the waitlist group: 1. Perceived stress (measured using the Perceived Stress Scale 10 items, PSS-10) 2. Quality of life (EuroQol 5 Dimensions 5 levels, EQ-5D-5L) 3. Wellbeing (ONS-4)

Secondary

MeasureTime frame
At Screening/Baseline, 10 weeks (end of intervention), 14 weeks, and 22 weeks for the intervention group and at Screening/Baseline, 10 weeks, 20 weeks (end of intervention, for those who choose to enrol in the intervention after the initial waitlist period), and 24 weeks for the waitlist group: 1. Anxiety (Generalized Anxiety Disorder-7 (GAD-7) 2. Sleep quality (PSQI-2) 3. Emotional regulation (Difficulties in Emotion Regulation Scale, DERS-16) 4. Self-esteem (Rosenberg Self-esteem Questionnaire, RSES)

Countries

Spain

Contacts

Public ContactMargarita Triguero-Mas
mtrigueroma@uoc.edu+34 93 326 36 00

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jul 31, 2026