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N/A Completed N=8 Supportive Care

Ready to Sail: Evaluating Sailing's Feasibility as Ergotherapy

Multiple Osteochondroma · Ollier Disease · osteogenesis imperfecta
Source: ClinicalTrials.gov NCT06397443 ↗
Enrolled (actual)
8
Serious AEs
0.0%
Results posted
Mar 2025
Primary outcomePrimary: Health-related Quality of Life — 0.91; 84 score on a scale

Summary

Background Individuals with rare skeletal disorders frequently experience psychological distress, social isolation, unmet needs, and significant challenges due to limited treatment options. Adventure Therapy, employing exposure to natural environments, has shown promise in improving self-esteem, autonomy, and social skills in chronic illness and disability populations. This pilot study explores the feasibility and preliminary efficacy of a sailing-based intervention for enhancing physical, social, and psychological well-being in this specific population. Outcome Measures The primary outcome is to investigates the feasibility of sailing to improve well-being and quality of life in patients living with rare skeletal disorders. Furthermore, the investigators hypothesize that participation in a sailing program led by occupational therapists will lead to improvements in: * Movement confidence: assessing whether sailing enhances participants' ability to move and perform daily activities. * Mental health: evaluating if sailing reduces anxiety and fear and promotes self-esteem. * Social interaction: exploring if sailing fosters social connection and reduces feelings of isolation. Methods The study will use a prospective, single-arm, longitudinal design. Eight participants with rare skeletal disorders will be enrolled in a 5-day sailing-based occupational therapy intervention. Comprehensive pre- and post-intervention assessments will measure psychosocial factors, quality of life, functional mobility, kinesiophobia, and body segment movement using questionnaires and functional scales.

Outcome Measures

OutcomeResultp-value
PRIMARY
Health-related Quality of Life
0.82; 83.50
PRIMARY
Health-related Quality of Life
0.82; 83.50
PRIMARY
Health-related Quality of Life
0.82; 83.50
PRIMARY
Health-related Quality of Life
0.82; 83.50
SECONDARY
Self-esteem
21
SECONDARY
Self-esteem
21
SECONDARY
Self-esteem
21
SECONDARY
Self-esteem
21
SECONDARY
Motor Coordination
12; 16; 28
SECONDARY
Motor Coordination
12; 16; 28
SECONDARY
Motor Coordination
12; 16; 28
SECONDARY
Motor Coordination
12; 16; 28
SECONDARY
Balance
56
SECONDARY
Balance
56
SECONDARY
Balance
56
SECONDARY
Balance
56
SECONDARY
Kinesiophobia
SECONDARY
Kinesiophobia
SECONDARY
Kinesiophobia
SECONDARY
Well-being and Mental Health
SECONDARY
Well-being and Mental Health
SECONDARY
Well-being and Mental Health
SECONDARY
Physical Functioning and Psychological Well-being
97.92; 96.97; 88.19; 67.22; 80; 85.73
SECONDARY
Physical Functioning and Psychological Well-being
97.92; 96.97; 88.19; 67.22; 80; 85.73
SECONDARY
Physical Functioning and Psychological Well-being
97.92; 96.97; 88.19; 67.22; 80; 85.73
SECONDARY
Physical Functioning and Psychological Well-being
97.92; 96.97; 88.19; 67.22; 80; 85.73

Eligibility Criteria

Inclusion Criteria

  • Individuals of any gender
  • Diagnosis of a rare skeletal disease, confirmed clinically and/or molecularly
  • Age 12 years or older
  • No history of surgery within six months prior to study enrollment.

Exclusion Criteria

  • Individuals undergoing diagnostic evaluation for a rare skeletal disease
  • Participants younger than 12 years of age.
  • Individuals who underwent surgery within the preceding 6 months.
  • Participants with fractures or musculoskeletal injuries sustained within the past year.
  • Individuals who were unable to provide written informed consent.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06397443). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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