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Behavioural Intervention

Guided Imagery Intervention for Health Behaviors

N/A

Waitlist Available

Led By Phyllis S Hansell

Research Sponsored by Seton Hall University

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Between the ages of 18-60

Be between 18 and 65 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up twenty-one days after the baseline, change will be measured over time

Awards & highlights

Study Summary

This trial is testing three different ways to improve women's overall health. The methods being tested include cognitive power training, guided imagery, and a combination of both. The goal is to compare these interventions with

Who is the study for?

This trial is for women interested in improving their functional health. The specific eligibility criteria are not provided, but typically participants would need to meet certain health and demographic requirements set by the study.Check my eligibility

What is being tested?

The study tests three interventions: Cognitive Power Intervention, Guided Imagery, and a combination of both. Women will be randomly assigned to one of these methods or a control group to see which is most effective at enhancing functional health.See study design

What are the potential side effects?

Since the interventions involve cognitive techniques and imagery rather than drugs or medical procedures, side effects may include discomfort with mental exercises but are generally expected to be minimal.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Select...

I am between 18 and 60 years old.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ at the baseline.the tool is nown as the power as knowing participation in change tool (pkpct).

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~at the baseline.the tool is nown as the power as knowing participation in change tool (pkpct).

This trial's timeline: 3 weeks for screening, Varies for treatment, and at the baseline.the tool is nown as the power as knowing participation in change tool (pkpct). for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Functional Health in Women

Power to Change in Women

Power to change in Women

Trial Design

4Treatment groups

Experimental Treatment

Active Control

Group I: Guided Imagery InterventionExperimental Treatment1 Intervention

Participants randomly assigned to this group will be provided with a MP3 Player which will have three guided imagery programs. The Guided Imagery Programs include: 1.Relaxation and Wellness; 2. Immune System Imagery and 3. Healing Trauma. The study measures are completed upon entry and 21 days post entry into the study and include: PKPCT and 21 days post entry into the study and include: PKPCT and the SF-36v2.

Group II: Combined Guided Imagery and Cognitive Power InterventionExperimental Treatment1 Intervention

The participants are randomly assigned to this group completes The Power as Knowing Participation in Change (PKPCT) and the Guided Imagery Intervention as described above. The study measures are completed upon entry and 21 days after entry and include the PKPCT and the SF-36v2.

Group III: Cognitive Power InterventionExperimental Treatment1 Intervention

The participant is randomly assigned to this group completes The Power as Knowing Participation in Change (PKPCT) to determine: 1. Freedom to Act Intentionally; 2. Involvement in creating change; 3.Freedom to act intestinally and 4. My involvement in creating change. The study measures are completed upon entry and 21 days post entry into the study and include: PKPCT and the SF-36v2.

Group IV: Control Group (No intervention)Active Control1 Intervention

The participants are randomly assigned to this group complete all study measures PKPCT and the SF-36v2 measures upon entry into the study and 21 days after entry.

Treatment

First Studied

Drug Approval Stage

How many patients have taken this drug

Guided Imagery

2010

N/A

~1010

0 / 1Eligibility criteria met

Find a Location

Who is running the clinical trial?

Seton Hall UniversityLead Sponsor

2 Previous Clinical Trials

113 Total Patients Enrolled

Phyllis S HansellPrincipal InvestigatorSeton Hall University

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What are the specific criteria for individuals to be eligible to enroll in this research investigation?

"To be eligible for participation in this trial, individuals must exhibit healthy behaviors and fall within the age range of 18 to 60. The study aims to recruit a total of 80 participants."

Answered by AI

Are there any available vacancies for participants in this clinical trial?

"As reported on clinicaltrials.gov, this particular medical trial is not currently accepting new participants. The trial was initially posted on February 1st, 2024 and recently updated on January 30th, 2024. However, it's important to note that there are still a total of 91 other ongoing clinical trials actively seeking eligible patients at this time."

Answered by AI

Does this clinical trial include individuals who are older than 85 years of age?

"To be considered eligible for this trial, individuals must fall within the age range of 18 to 60. Please note that there are separate studies available for participants under the age of 18 (36 studies) and those over the age of 65 (61 studies)."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

A Pilot Intervention Study to Promote Functional Health in Women

Phyllis Hansell 2024. "A Pilot Intervention Study to Promote Functional Health in Women". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT06235255.