NCT07609563

Brief Summary

This study looks at whether therapeutic climbing - indoor climbing activities guided by therapists - can help children with Developmental Coordination Disorder (DCD). DCD is a condition where children have difficulty with motor skills and participation in everyday activities, and sometimes confidence in physical activities. The climbing program is based on a problem-solving approach called CO-OP (Cognitive Orientation to daily Occupational Performance), in which children learn strategies to achieve goals.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 12, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

May 15, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

May 27, 2026

Completed
10 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 6, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 6, 2026

Completed
Last Updated

June 1, 2026

Status Verified

May 1, 2026

Enrollment Period

22 days

First QC Date

May 12, 2026

Last Update Submit

May 27, 2026

Conditions

Keywords

Therapeutic climbingNeurodevelopmental conditionGroup interventionParticipation-oriented approachOccupational therapy

Outcome Measures

Primary Outcomes (3)

  • Performance related to individualized goals

    Assess with the Canadian Occupational Performance Measure (COPM) (visual analog scale of 1-10)

    Baseline (2-3 months before the intevention, pre-intervention (immediatly before the intervention), post-intervention (immediatly after the intervention), follow-up 2-3 months post-intervention

  • Satisfaction related to individualized goals

    Assess with the Canadian Occupational Performance Measure (COPM) (visual analog scale of 1-10)

    Baseline (2-3 months before the intervention, pre-intervention (immediatly before the intervention), post-intervention (immediatly after the intervention), follow-up 2-3 months post-intervention

  • Performance related to climbing-specific goals

    Assess with the Performance Quality Rating Scale (PQRS) (visual analog scale of 1-10)

    Baseline (2-3 months before the intervention, pre-intervention (immediatly before the intervention), post-intervention (immediatly after the intervention), follow-up 2-3 months post-intervention

Secondary Outcomes (4)

  • Motor skills

    Baseline (2-3 months before the intervention, pre-intervention (immediatly before the intervention), post-intervention (immediatly after the intervention), follow-up 2-3 months post-intervention

  • Self-efficacy

    Baseline (2-3 months before the intervention, pre-intervention (immediatly before the intervention), post-intervention (immediatly after the intervention), follow-up 2-3 months post-intervention

  • Executive functioning

    Baseline (2-3 months before the intervention, pre-intervention (immediatly before the intervention), post-intervention (immediatly after the intervention), follow-up 2-3 months post-intervention

  • Motivation for physical activity

    Baseline (2-3 months before the intervention, pre-intervention (immediatly before the intervention), post-intervention (immediatly after the intervention), follow-up 2-3 months post-intervention

Study Arms (2)

Group 1 - Fall 2026

EXPERIMENTAL

First group intervention

Other: CO-OP-based group therapeutic climbing intervention

Group 2 - Winter 2027

EXPERIMENTAL

Second group intervention

Other: CO-OP-based group therapeutic climbing intervention

Interventions

The intervention will consist of a 10-week group-based therapeutic climbing program delivered once weekly on Saturday afternoons at an indoor climbing center. Sessions will be delivered by an occupational therapist (OT), two occupational therapy interns, and a certified climbing monitor (hereafter referred to as "intervention providers"). Each 90-minute session will follow the same global structure. The intervention is grounded in the CO-OP approach.

Group 1 - Fall 2026Group 2 - Winter 2027

Eligibility Criteria

Age8 Years - 12 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Diagnosis of DCD by a physician\*.
  • Ability to follow instructions, communicate verbally, interact with adults and peers, and use cognitive strategies.
  • Ability to attend all assessment and intervention sessions in Sherbrooke.
  • Ability to understand and speak French.
  • Provision of child assent and parental consent. \* If the target sample size (n = 16) is not reached, children with suspected DCD based on the Developmental Coordination Disorder Questionnaire (DCDQ) (25,26) will also be considered. Eligibility will then require: (1) a score below the 15th percentile on the total motor composite or below the 5th percentile in a domain of the Bruininks-Oseretsky Test of Motor Proficiency (BOT) (27,28), and (2) the identification of occupational challenges using the Canadian Occupational Performance Measure (COPM) (29,30) during the initial assessment.

You may not qualify if:

  • Diagnosis of severe behavioral disorders, autism spectrum disorder, intellectual disability, cerebral palsy, muscular dystrophy, and/or severe functional limitations.
  • Prior proficiency in climbing or absence of climbing-related goals.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Motor Skills Disorders

Condition Hierarchy (Ancestors)

Neurodevelopmental DisordersMental Disorders

Study Officials

  • Emmanuelle Jasmin, Ph.D.

    Université de Sherbrooke

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Emmanuelle Jasmin, Ph.D.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 12, 2026

First Posted

May 27, 2026

Study Start

May 15, 2026

Primary Completion

June 6, 2026

Study Completion

June 6, 2026

Last Updated

June 1, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share