Active rocking in a rocking chair
BehavioralParticipants will actively rock 3 times per day for 30 minutes in a rocking chair
Other names: Rocking
NCT Number: NCT07544550
Feasibility and acceptability randomized controlled trial exploring the use of a rocking chair after a total hip arthroplasty in adults who are aged 65 or older. Primary aims include its feasibility and acceptability; exploratory aims include the impact of rocking on pain, gastrointestinal effects, anxiety, ambulation, and additional healthcare visits.
Trial opening soon.
Get Notified65 year and older
All sexes
Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will actively rock 3 times per day for 30 minutes in a rocking chair
Other names: Rocking
Participants will sit upright in a stationary chair 3 times per day for 30 minutes
Other names: Sitting
Time frame: From enrollment to 31-day follow-up
Feasibility of active rocking post-operative measured by total number of participants enrolled, total percentage and number completing the study, and percent of missing data. A higher percent of missing data is a negative outcome.
Time frame: From enrollment to 31-day follow-up
Acceptability of rocking or sitting after hip arthroplasty indicated by score on domains of affective, perceived effectiveness, intervention coherence, ethicality, burden, opportunity costs, self-efficacy likert scales from 1-4 (Not at all, a little, somewhat, very much). Scores from each domain are combined and summed to determine a single acceptability score (higher scores equate to higher acceptability of the intervention).
Time frame: From surgery (Day 1 of the study) to 31-day follow-up
Participants indicate Daily nausea assessment on 5-point Likert scale (never, rarely, sometimes, often, always). Higher scores indicate more Nausea.
Time frame: From surgery (Day 1 of the study) to end of 31-day follow-up
Participants reporting Daily gas/bloating assessment on 5-point Likert scale (not at all, a little bit, somewhat, quite a bit, very much). Higher scores indicate more daily gas/bloating.
Time frame: From surgery (Day 1 of the study) to end of 31-day follow-up
Participants reporting Daily pain assessment on 5-point likert scale (no pain, mild, moderate, severe, very severe). Higher scores equate to more daily pain experienced.
Time frame: After surgery (Day 1 of the study) and up to 7 days post-surgery
The amount of participants' Daily ambulation will be assessed with the amount of steps taken per day using the triaxial accelerometer activPAL4pro. More steps per day equates to greater ambulation.
Time frame: From enrollment through 31-day follow-up
The participants will report their Daily anxiety assessment using the Anxiety subscale of the Neuro-QoL Hospital Anxiety and Depression Scale, which assesses self-reported fear, worry, tension, and nervousness and will be scored with a T-score with higher scores indicating more anxiety. The scores range from 0-3 (not at all, not often, sometimes, most of the time).
Time frame: From surgery (Day 1 of the study) until 31-day follow-up
The total number of Additional healthcare visits will be assessed via phone call at 31-days post-surgery using the investigator-developed question: Have you been hospitalized since you have been discharged from your hip surgery?
Contact information is provided by the study sponsor or research team.
University of Missouri, Kansas City
Other
Feasibility and Acceptability of the Impact of a Rocking Chair Intervention on Recovery Compared to Standard Care of Stationary Chair on Older Adults After Elective Orthopedic Hip Surgery: A Randomized Controlled Trial
Acronym: FAIRChair
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07625033
Anesthesia, Aortic Valve Replacement
Metz, France
View Trial DetailsNCT07649642
Clinical Deterioration, Deterioration, Clinical
Copenhagen, Denmark
View Trial DetailsNCT07631819
Joint Diseases, Joint Instability
View Trial DetailsNCT07612202
Postoperative Care, Prolapse Genital
Hillerød, Copenhagen, Denmark
View Trial Details