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Maximising shoulder function following accessory nerve damage (neurapraxia) after neck dissection surgery for cancer

Effect of a progressive resisted exercise program on shoulder pain and function following accessory nerve neurapraxia after neck dissection surgery for cancer

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000066987
Enrollment
59
Registered
2011-01-19
Start date
2009-04-01
Completion date
2012-09-15
Last updated
2021-03-16

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

Conditions

None listed

Brief summary

This study looks at the effect of a progressive exercise program on shoulder pain and function following nerve injury after neck dissection surgery for cancer. Who is it for? You can join this study if you have undergone neck dissection surgery for head and neck cancer within eight weeks and you have clinical signs of injury to the accessory nerve which includes weakness of shoulder movements. Trial details Participants will be randomly divided into two groups. One group (control) will receive standard care (physiotherapy or a handout of generalised exercises and advice about scar care). The other group will attend the physiotherapy department for a supervised exercise program. This involves progressive strengthening exercises for half an hour, once a week for 12 weeks, with the same exercises performed at home twice a week. Assessments will be carried out at the start of the study and at 3, 6 and 12 months. The study aims to compare levels of pain, disability and shoulder movement in the different groups.

Interventions

Participants eligible are those that have undergone neck dissection surgery for cancer within eight weeks, that present with clinical signs of accessory nerve injury; dropped scapula, winged scapula, and reduced active abduction on the operated side. Participation in the intervention group will involve attending the physiotherapy department at the study sites for a supervised exercise program. This involves progressive strengthening exercises using hand weights, active-assisted range of movement

Participants eligible are those that have undergone neck dissection surgery for cancer within eight weeks, that present with clinical signs of accessory nerve injury; dropped scapula, winged scapula, and reduced active abduction on the operated side. Participation in the intervention group will involve attending the physiotherapy department at the study sites for a supervised exercise program. This involves progressive strengthening exercises using hand weights, active-assisted range of movement exercises of the shoulder, active range of movement exercises of the neck, and stretches of the shoulder and neck. The supervising physiotherapist ensures no worsening of pain or fatigue occurs during sessions. This will take half an hour, once a week for 12 weeks. The same exercises will be performed at home twice a week. Exercise diaries are utilised to ensure compliance and no self upgrading of exercises.

Sponsors

Calvary Mater Newcastle
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Must be within 8 weeks of neck dissection surgery, with accessory nerve preservation and scar fully healed.

Exclusion criteria

Non English speaking, that requires an interpreter. Metastases to other areas. Does not possess ability to give informed consent. Nil cognitive impairment, intellectual disability or significant mental illness. Not pregnant.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026