Patient Education and Sling Use After Shoulder Surgery
Evaluation of Educational Pamphlets and Female Patient Experience With Post-operative Sling-Wear
This study will evaluate whether educational pamphlets can help patients safely manage personal hygiene, household activities, and female-specific self-care while wearing a sling after surgery. The study will also examine whether following sling-use instructions is associated with better short-term recovery and patient-reported outcomes for up to 6 months after surgery.
Studieöversikt
Status
Betingelser
Studietyp
Inskrivning (Beräknad)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, Förenta staterna, 19107
- Rothman Orthopaedic Institute
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Participants scheduled to undergo shoulder surgery at Rothman Orthopaedics that requires more than 1 week of postoperative shoulder sling use.
- Participants who are able to provide informed consent.
- Participants who have sufficient English-language proficiency to understand the study materials and complete the study questionnaires.
Exclusion Criteria:
- Participants undergoing shoulder surgery that does not require more than 1 week of postoperative shoulder sling use.
- Participants who do not have sufficient English-language proficiency to understand the study materials and complete the study questionnaires.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Control Group - Standard postoperative education
Standard postoperative education |
Participants will receive the standard postoperative education and instructions provided by their treating orthopedic physician for patients undergoing shoulder surgery requiring postoperative sling use. |
|
Aktiv komparator: Pamphlet Intervention Group
Standard postoperative education + "Living with a Sling" educational pamphlets |
Participants will receive standard postoperative education plus educational pamphlets providing guidance on performing daily activities while wearing a shoulder sling. The pamphlets address personal hygiene, household tasks, and self-care. Female participants will also receive a pamphlet addressing female-specific self-care. |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Sling adherence
Tidsram: 4 to 6 weeks after surgery
|
Sling adherence will be assessed using patient-reported survey responses regarding adherence to prescribed shoulder sling use during the postoperative period. |
4 to 6 weeks after surgery
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Patient-reported shoulder function
Tidsram: 6 months after surgery
|
Shoulder function will be assessed using the American Shoulder and Elbow Surgeons (ASES) score. |
6 months after surgery
|
Andra resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Patient-reported shoulder status
Tidsram: 6 months after surgery
|
Patient-reported shoulder status will be assessed using the Single Assessment Numeric Evaluation (SANE). |
6 months after surgery
|
|
Patient experience while wearing a shoulder sling
Tidsram: 6 weeks after surgery
|
Participants will complete a questionnaire assessing their experience performing daily activities, including personal hygiene, household tasks, and self-care while wearing a shoulder sling. |
6 weeks after surgery
|
|
Preparedness for postoperative activities
Tidsram: 6 weeks after surgery
|
Participants will report their preparedness and ability to manage daily activities while wearing a shoulder sling. |
6 weeks after surgery
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- MBIS2024-1306
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