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Compares treatment options for Solid Cancers
Official title The Effect of Using Weighted Blanket on Anxiety, Stress, Depression and Comfort Level Among Patients With Cancer Undergoing Intravenous Anticancer Therapy and Its Feasibility of Use by Nurses Compared to Routine Care
ClinicalTrials.gov ID: NCT07653035
What this study is testing
- What it's testing
- Protocol Title: Protocol Title: The Effect of using Weighted Blanket on anxiety, stress, depression and comfort level among Patients with cancer undergoing intravenous (IV) anticancer therapy and its feasibility of use by nurses compared to routine care; a Randomized controlled study. Study Tools: VAS-A, ESAS-R, DASS-21 and comfort level scale will be used to study the patients' population.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- for patients
- Newly diagnosed cancer patients aged 18 years and older.
- Receiving first-line intravenous anticancer therapy (chemotherapy or immunotherapy or a combination of both) in the daycare unit (adjuvant...
- Weighting at least 55 kg during obtaining the informed consent. (At least 54 kg before the intervention).
- Able to complete study assessments.
You likely can't join if
- for patients:
- Prior psychological treatment or psychotherapy (confirmed psychological diagnosis, history of psychotropic medications and previous psychotherapy).
- Currently hospitalized in inpatient units.
- Patients on daily anticancer infusions.
- Positive fall risk assessment.
- Open wounds and recent surgeries/ stoma.
See the full eligibility criteria
- for patients
- Newly diagnosed cancer patients aged 18 years and older.
- Receiving first-line intravenous anticancer therapy (chemotherapy or immunotherapy or a combination of both) in the daycare unit (adjuvant, neoadjuvant, or palliative).
- Weighting at least 55 kg during obtaining the informed consent. (At least 54 kg before the intervention).
- Able to complete study assessments.
- Speaks Arabic or English.
- Signs Informed consent.
- for patients:
- Prior psychological treatment or psychotherapy (confirmed psychological diagnosis, history of psychotropic medications and previous psychotherapy).
- Currently hospitalized in inpatient units.
- Patients on daily anticancer infusions.
- Positive fall risk assessment.
- Open wounds and recent surgeries/ stoma.
- Enrolled in any other device study or clinical trial during data collection.
- History of:
- Diabetes mellitus
- Respiratory disorders,
- Claustrophobia (Miller et al 2003) Because of the possibility for altered sensory perception,
- Patients who had a diagnosis of peripheral neuropathy or fibromyalgia (Vinson et al. 2020)
- Cognitive impairment Eligibility criteria for the nurse's population: Day Care Unit nurses will be recruited by convenient sampling and feedback will be sought per patient per visit. The reason to this is because the...
The study team makes the final eligibility decision.
Where it's taking place
- Muscat, Seeb, Oman
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Muscat, Seeb, Oman. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.