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Chin tuck against resistance with feedback: swallowing rehabilitation in frail older people admitted to hospital with pneumonia. A feasibility randomised controlled study of two types of rehabilitation exercise using chin tuck against resistance to improve swallowing, eating and drinking

Chin tuck against resistance with feedback: swallowing rehabilitation in frail older people admitted to hospital with pneumonia. A feasibility randomised controlled study of two types of rehabilitation exercise using chin tuck against resistance to improve swallowing, eating and drinking

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12813363
Enrollment
60
Registered
2020-02-06
Start date
2021-06-08
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Swallowing problems in frail older people Digestive System

Interventions

People will be recruited when they are medically safe to be so, from Acute Frailty wards/Units at Queen Elizabeth Hospital and Southmead Hospital. When they agree to take part, consent will be sought.

Sponsors

Lewisham and Greenwich NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Medically stable (systolic BP > 110; Heart rate > 60 bpm, MEWS = 4 14 5. Able to provide consent (Different media will be provided to patients to enable consent to occur e.g. pictures; Speech Therapy support) 6. No significant breathlessness (St Georges COPD Score) 7. Not requiring oxygen 8. No past history of stroke or neurological disease 9. No evidence of severe rheumatoid arthritis (risk of neck instability)

Exclusion criteria

Exclusion criteria: 1. Failure to provide consent to take part in the study 2. Progressive medical conditions (some malignancy, neurological disease) 3. MoCA < 14 4. Dysphagia requiring active intervention at the time of assessment 5. Dysphagia secondary to surgical treatment of head and neck cancer

Design outcomes

Primary

MeasureTime frame
1. Recruitment rates across two NHS hospital sites assessed using the number recruited per month and the total in the study period recorded using REDcap trial management software 2. Willingness to be recruited to the study assessed using the number of people who refuse and their reasons for refusing recorded using REDcap trial management software 3. Study retention (<30% drop out) assessed using number not completing the study relative to the number agreeing to participate recorded using REDcap trial management software 4. Compliance: 80% of exercises undertaken daily assessed using the Exerphager app, which will show the exercise data for all sessions completed 5. The absence of adverse incidents assessed using the number of reports using REDcap trial management software 6. Acceptability of intervention assessed using a 5-point questionnaire 7. Mechanics of swallowing assessed using videofluoroscopy (reduced PTT; reduced residue post swallow) 8. Aspiration prevention assessed by analysing laryngeal movement, UES opening and tongue base retraction visualised using videofluoroscopy 9. Swallow speed assessed using TWST (time taken to drink 90 ml of water) 10. Ease of use of the CTAR-SwiFt feedback system assessed using using verbal feedback and the Swift-ball usability questionnaire 11. Swallowing ability assessed using FOIS (food oral intake score). It is scored between 1 and 7. 0 refers to being unable to eat or drink. 7 is normal diet. This is completed by medical staff. 12. Dysphagia-related quality of life assessed using the Swal-Qol questionnaire 13. Health status assessed using the EQ-5D questionnaire 14. Strength and mobility assessed using Timed Up and Go test. Participants must stand from sitting, walk 3 m, then turn around, walk back to the chair and sit down again. All measures are assessed at baseline, 12 weeks and 24 weeks.

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 18, 2026