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Not yet recruiting NCT07504874

The Effect of Gardening Activities on the Quality of Life of Students With Mild Intellectual Disability

No phase Interventional Intellectual Disability Quality of Life

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Horticultural activity.
Who it may be relevant to
Registry conditions: Intellectual Disability, Quality of Life. Basic parameters: 11 years — 14 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Gardening Activities on the Quality of Life of Mildly Intellectually Disabled Secondary School Students: A Mixed-Method Study

Overview

This study will be conducted to determine the effect of gardening activities applied to mildly intellectually disabled secondary school students on their quality of life and to examine their views on these activities in depth.

Interventions

  • Behavioral Horticultural activity
    Students will participate in structured gardening activities once a week for 8 weeks, approximately 40 minutes per session, under supervision in a school greenhouse.

Primary outcome measures

  • KINDL Quality of Life Scale - Parent Form [Time frame: Day 0- Mounth 2]

Eligibility criteria

Inclusion criteria

  • Students studying at a special education secondary school,
  • Who are open to communication and collaboration,
  • Who have no physical or mental disabilities that would prevent them from participating in gardening activities,
  • And whose parents have provided written informed consent for their participation will be included in the research.

Exclusion criteria

  • Students who do not attend the educational program regularly will be excluded from the research.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07504874 · ORDU-SABE-ST-02

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗