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Torticollis in infants due to suboccipital strain: a pilot study

Torticollis in infants due to suboccipital strain: a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10734062
Enrollment
30
Registered
2007-10-16
Start date
2007-05-02
Completion date
Unknown
Last updated
2021-07-26

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

Conditions

Torticollis in infancy Musculoskeletal Diseases Dorsopathies

Interventions

Group 1: receives manual therapy once or twice in addition to child physiotherapy. Manual therapy will take place at the first visit, and then again in four weeks time if necessary. Gr

Sponsors

Akershus University Hospital (Akershus Universitetssykehus) (Norway)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Infants with torticollis, aged 3 - 6 months 2. Active and passive range of movement of the neck must be restricted

Exclusion criteria

Exclusion criteria: 1. Serious pathology - somatic and cognitive 2. Syndromes 3. Intermittent torticollis

Design outcomes

Primary

MeasureTime frame
Each infant is videotaped three times during the study period of eight weeks. The films are assessed by three child physiotherapists and scored individually into five different categories due to the seriousness of the torticollis. Primary and secondary outcomes will be measured at the first visit, after 2 weeks and at last after 8 weeks. The randomisation then ends and both groups can get manual therapy if it is needed.

Secondary

MeasureTime frame
1. Active range of movement of the neck 2. Compensations during active rotation of the neck 3. Passive range of movement of the neck (rotation, lateral and ventral flexion) 4. Signs of pain when passive range of movement is tested 5. Antigravity movement of the neck during lateral tilting of the infant 6. Anamnestic information 7. Questionnaire: this questionnaire is in Norwegian, and consists of seven questions with a Visual Analog Scale line Primary and secondary outcomes will be measured at the first visit, after 2 weeks and at last after 8 weeks. The randomisation then ends and both groups can get manual therapy if it is needed.

Countries

Norway

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026