- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05660148
Influence of Resentment and Forgivingness on Quality of Life in People Living With HIV (FORGHIV)
May 27, 2026 updated by: Centre Hospitalier Universitaire, Amiens
Life stress is strongly associated with poor mental and physical health and its effects explain significant morbidity and mortality.
Forgiveness is one of the factors that can influence the effects of stress on health.
By definition, forgiveness is the release of negative feelings, emotions, and behaviors - and possibly the release of positive feelings - toward an offender.
Numerous studies have shown that forgiveness is associated with several mental and physical health benefits.
The literature argues that high levels of propensity to forgive (trait) predispose that person to experience forgiveness (state) more often.
In other words, a stronger forgiving disposition is believed to increase the experience of forgiveness, which, in turn, mitigates the negative effects of stress.
Forgiveness is therefore a coping style that can play a beneficial role in the stress-health relationship.
Patients living with HIV (PLHIV) are patients particularly exposed to stress, not only because of their chronic pathology but also because of the stigma attached to this disease.
Very few studies have studied the impact of forgiveness (state or trait) on the physical health of PLHIV and even fewer the impact of an intervention promoting the disposition to forgive.
The objective of this prospective observational monocentric study is to show in a very secular country that forgiveness has an effect on well-being as well as on other health parameters.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
206
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jean-Philippe Lanoix, Pr
- Phone Number: 03 22 08 80 51
- Email: lanoix.jean-philippe@chu-amiens.fr
Study Locations
-
-
-
Amiens, France, 80480
- Recruiting
- CHU Amiens
-
Contact:
- Jean-Philippe Lanoix, MD
- Phone Number: (33)3 22 66 88 13
- Email: lanoix.jean-philippe@chu-amiens.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients living with HIV (PLHIV) are patients particularly exposed to stress, not only because of their chronic pathology but also because of the stigma attached to this disease.Patients belonging to the PLHIV followed at the Amiens University Hospital, not likely to move within the year
Description
Inclusion Criteria:
- Belonging to the PLHIV followed at the Amiens University Hospital, not likely to move within the year
- Possibility of follow-up in teleconsultation (usual support of the service)
- Benefiting from a social security scheme
- Consent to participate in the research
Exclusion Criteria:
- Erratic follow-up (non-compliance, predictable move) or moribund patient
- Illiterate or not speaking french
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
establishment of correlation between the inclination to forgiveness and the quality of life
Time Frame: 18 months
|
18 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 6, 2024
Primary Completion (Estimated)
November 6, 2026
Study Completion (Estimated)
November 6, 2026
Study Registration Dates
First Submitted
December 13, 2022
First Submitted That Met QC Criteria
December 13, 2022
First Posted (Actual)
December 21, 2022
Study Record Updates
Last Update Posted (Actual)
May 28, 2026
Last Update Submitted That Met QC Criteria
May 27, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Blood-Borne Infections
- Urogenital Diseases
- Genital Diseases
- Immune System Diseases
- Infections
- RNA Virus Infections
- Virus Diseases
- Communicable Diseases
- Sexually Transmitted Diseases, Viral
- Sexually Transmitted Diseases
- Lentivirus Infections
- Retroviridae Infections
- Immunologic Deficiency Syndromes
- Slow Virus Diseases
- HIV Infections
- Behavior
- Social Behavior
- Acquired Immunodeficiency Syndrome
- Social Stigma
Other Study ID Numbers
- PI2022_843_0010
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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