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Recruiting NCT06507072

Adaptive Rock Climbing

No phase Interventional Congenital Upper Limb Differences

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: Adaptive Rock Climbing Program.
Who it may be relevant to
Registry conditions: Congenital Upper Limb Differences. Basic parameters: 6 years — 16 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
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Evaluating Adaptive Rock Climbing on Children With Upper Limb Differences

Overview

The goal of this clinical trial is to assess changes in functional and psychosocial outcomes following a 12-week adaptive rock-climbing program for children with congenital upper limb differences. The main questions it aims to answer are * Assess functional outcomes following a 12-week adaptive rock-climbing program. * Assess psychosocial outcomes following a 12-week adaptive rock climbing program. * Assess barriers to participation in adaptive sports. Participants will complete 12-week adaptive rock climbing program.

Interventions

  • Behavioral Adaptive Rock Climbing Program
    Twelve week rock climbing program. The program will take place once per week over the course of twelve weeks.

Primary outcome measures

  • Change from Baseline in Range of Motion at 12 Weeks [Time frame: Baseline and 12 weeks]
  • Change from Baseline in KINDL Scores at 12 Weeks [Time frame: Baseline and 12 weeks]
  • Change from Baseline in Muscle Testing at 12 Weeks. [Time frame: Baseline and 12 weeks]
  • Change from Baseline in PROMIS Life Satisfaction Scores at 12 Weeks. [Time frame: Baseline and 12 weeks]
  • Change from Baseline in PROMIS Pediatric Global Health Scores at 12 Weeks [Time frame: Baseline and 12 weeks]
Secondary outcome measures (1)
  • Assess Barriers to Participation in Adaptive Sports [Time frame: At 12 weeks (post-intervention)]

Eligibility criteria

Inclusion criteria

  • Parents 18 years and older.
  • English or Spanish speaking.
  • Participants with unilateral or bilateral congenital upper extremity disorders of limb formation differences ages 6-16.

Exclusion criteria

  • Any patients younger than 6 years or older than 16 years, patients not fluent in English or Spanish, or patients with parents younger than 18 years.

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

Healthy volunteers: No

Study design

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

Study locations

United States · 1 center
  • Children Hospital Los Angeles — Los Angeles

Identifiers

NCT: NCT06507072 · CHLA-24-00150

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗